SCN1A (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "SCN1A" in English language version.

refsWebsite

Global rank English rank

36nih.gov

4^th place

23doi.org

2^nd place

6semanticscholar.org

11^th place

8^th place

3harvard.edu

18^th place

17^th place

2ensembl.org

1,626^th place

1,007^th place

2web.archive.org

1^st place

1ua.ac.be

low place

1lovd.nl

low place

1scn1a.info

low place

1smh.com.au

132^nd place

96^th place

doi.org (Global: 2^nd place; English: 2^nd place)

Malo MS, Blanchard BJ, Andresen JM, Srivastava K, Chen XN, Li X, et al. (1994). "Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24". Cytogenetics and Cell Genetics. 67 (3): 178–186. doi:10.1159/000133818. PMID 8062593.
Ito M, Nagafuji H, Okazawa H, Yamakawa K, Sugawara T, Mazaki-Miyazaki E, et al. (January 2002). "Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A". Epilepsy Research. 48 (1–2): 15–23. doi:10.1016/S0920-1211(01)00313-8. PMID 11823106. S2CID 25555020.
Catterall WA, Goldin AL, Waxman SG (December 2005). "International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels". Pharmacological Reviews. 57 (4): 397–409. doi:10.1124/pr.57.4.4. PMID 16382098. S2CID 7332624.
Meisler MH, O'Brien JE, Sharkey LM (June 2010). "Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects". The Journal of Physiology. 588 (Pt 11): 1841–1848. doi:10.1113/jphysiol.2010.188482. PMC 2901972. PMID 20351042.
Ogiwara I, Miyamoto H, Morita N, Atapour N, Mazaki E, Inoue I, et al. (May 2007). "Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation". The Journal of Neuroscience. 27 (22): 5903–5914. doi:10.1523/JNEUROSCI.5270-06.2007. PMC 6672241. PMID 17537961.
Tate SK, Depondt C, Sisodiya SM, Cavalleri GL, Schorge S, Soranzo N, et al. (April 2005). "Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin". Proceedings of the National Academy of Sciences of the United States of America. 102 (15): 5507–5512. Bibcode:2005PNAS..102.5507T. doi:10.1073/pnas.0407346102. PMC 556232. PMID 15805193.
Carvill GL, Engel KL, Ramamurthy A, Cochran JN, Roovers J, Stamberger H, et al. (December 2018). "Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies". American Journal of Human Genetics. 103 (6): 1022–1029. doi:10.1016/j.ajhg.2018.10.023. PMC 6288405. PMID 30526861.
Long YS, Zhao QH, Su T, Cai YL, Zeng Y, Shi YW, et al. (November 2008). "Identification of the promoter region and the 5'-untranslated exons of the human voltage-gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5'-untranslated exons". Journal of Neuroscience Research. 86 (15): 3375–3381. doi:10.1002/jnr.21790. PMID 18655196. S2CID 33673297.
Goldin AL, Snutch T, Lübbert H, Dowsett A, Marshall J, Auld V, et al. (October 1986). "Messenger RNA coding for only the alpha subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes". Proceedings of the National Academy of Sciences of the United States of America. 83 (19): 7503–7507. Bibcode:1986PNAS...83.7503G. doi:10.1073/pnas.83.19.7503. PMC 386747. PMID 2429308.
George AL, Komisarof J, Kallen RG, Barchi RL (February 1992). "Primary structure of the adult human skeletal muscle voltage-dependent sodium channel". Annals of Neurology. 31 (2): 131–137. doi:10.1002/ana.410310203. PMID 1315496. S2CID 37892568.
Gellens ME, George AL, Chen LQ, Chahine M, Horn R, Barchi RL, et al. (January 1992). "Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel". Proceedings of the National Academy of Sciences of the United States of America. 89 (2): 554–558. Bibcode:1992PNAS...89..554G. doi:10.1073/pnas.89.2.554. PMC 48277. PMID 1309946.
Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, et al. (April 2000). "Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2". Nature Genetics. 24 (4): 343–345. doi:10.1038/74159. PMID 10742094.
Lossin C (February 2009). "A catalog of SCN1A variants". Brain & Development. 31 (2): 114–130. doi:10.1016/j.braindev.2008.07.011. PMID 18804930.
Fujiwara T, Sugawara T, Mazaki-Miyazaki E, Takahashi Y, Fukushima K, Watanabe M, et al. (March 2003). "Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures". Brain. 126 (Pt 3): 531–546. doi:10.1093/brain/awg053. PMID 12566275.
Ohmori I, Kahlig KM, Rhodes TH, Wang DW, George AL (October 2006). "Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy". Epilepsia. 47 (10): 1636–1642. doi:10.1111/j.1528-1167.2006.00643.x. PMID 17054685.
Kohrman DC, Smith MR, Goldin AL, Harris J, Meisler MH (October 1996). "A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting". The Journal of Neuroscience. 16 (19): 5993–5999. doi:10.1523/JNEUROSCI.16-19-05993.1996. PMC 6579185. PMID 8815882.
Bulman DE (1997). "Phenotype variation and newcomers in ion channel disorders". Human Molecular Genetics. 6 (10): 1679–1685. doi:10.1093/hmg/6.10.1679. PMID 9300659.
Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P (June 2001). "De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy". American Journal of Human Genetics. 68 (6): 1327–1332. doi:10.1086/320609. PMC 1226119. PMID 11359211.
Yu FH, Mantegazza M, Westenbroek RE, Robbins CA, Kalume F, Burton KA, et al. (September 2006). "Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy". Nature Neuroscience. 9 (9): 1142–1149. doi:10.1038/nn1754. PMID 16921370.
Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, et al. (April 2000). "Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2". Nature Genetics. 24 (4): 343–345. doi:10.1038/74159. PMID 10742094. S2CID 29543172.
Spampanato J, Escayg A, Meisler MH, Goldin AL (October 2001). "Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2". The Journal of Neuroscience. 21 (19): 7481–7490. doi:10.1523/jneurosci.21-19-07481.2001. PMC 6762922. PMID 11567038.
Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, et al. (June 2003). "Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy". Neurology. 60 (12): 1961–1967. doi:10.1212/01.wnl.0000069463.41870.2f. PMID 12821740. S2CID 604240.
Gee SH, Madhavan R, Levinson SR, Caldwell JH, Sealock R, Froehner SC (January 1998). "Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins". The Journal of Neuroscience. 18 (1): 128–137. doi:10.1523/jneurosci.18-01-00128.1998. PMC 6793384. PMID 9412493.

ensembl.org (Global: 1,626^th place; English: 1,007^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000144285 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000064329 – Ensembl, May 2017

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Tate SK, Depondt C, Sisodiya SM, Cavalleri GL, Schorge S, Soranzo N, et al. (April 2005). "Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin". Proceedings of the National Academy of Sciences of the United States of America. 102 (15): 5507–5512. Bibcode:2005PNAS..102.5507T. doi:10.1073/pnas.0407346102. PMC 556232. PMID 15805193.
Goldin AL, Snutch T, Lübbert H, Dowsett A, Marshall J, Auld V, et al. (October 1986). "Messenger RNA coding for only the alpha subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes". Proceedings of the National Academy of Sciences of the United States of America. 83 (19): 7503–7507. Bibcode:1986PNAS...83.7503G. doi:10.1073/pnas.83.19.7503. PMC 386747. PMID 2429308.
Gellens ME, George AL, Chen LQ, Chahine M, Horn R, Barchi RL, et al. (January 1992). "Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel". Proceedings of the National Academy of Sciences of the United States of America. 89 (2): 554–558. Bibcode:1992PNAS...89..554G. doi:10.1073/pnas.89.2.554. PMC 48277. PMID 1309946.

lovd.nl (Global: low place; English: low place)

databases.lovd.nl

"The SCN1A gene homepage". Leiden Open Variation Database (LOVD). Leiden University Medical Center.

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Malo MS, Blanchard BJ, Andresen JM, Srivastava K, Chen XN, Li X, et al. (1994). "Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24". Cytogenetics and Cell Genetics. 67 (3): 178–186. doi:10.1159/000133818. PMID 8062593.
Ito M, Nagafuji H, Okazawa H, Yamakawa K, Sugawara T, Mazaki-Miyazaki E, et al. (January 2002). "Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A". Epilepsy Research. 48 (1–2): 15–23. doi:10.1016/S0920-1211(01)00313-8. PMID 11823106. S2CID 25555020.
Catterall WA, Goldin AL, Waxman SG (December 2005). "International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels". Pharmacological Reviews. 57 (4): 397–409. doi:10.1124/pr.57.4.4. PMID 16382098. S2CID 7332624.
Meisler MH, O'Brien JE, Sharkey LM (June 2010). "Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects". The Journal of Physiology. 588 (Pt 11): 1841–1848. doi:10.1113/jphysiol.2010.188482. PMC 2901972. PMID 20351042.
Ogiwara I, Miyamoto H, Morita N, Atapour N, Mazaki E, Inoue I, et al. (May 2007). "Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation". The Journal of Neuroscience. 27 (22): 5903–5914. doi:10.1523/JNEUROSCI.5270-06.2007. PMC 6672241. PMID 17537961.
Tate SK, Depondt C, Sisodiya SM, Cavalleri GL, Schorge S, Soranzo N, et al. (April 2005). "Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin". Proceedings of the National Academy of Sciences of the United States of America. 102 (15): 5507–5512. Bibcode:2005PNAS..102.5507T. doi:10.1073/pnas.0407346102. PMC 556232. PMID 15805193.
Carvill GL, Engel KL, Ramamurthy A, Cochran JN, Roovers J, Stamberger H, et al. (December 2018). "Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies". American Journal of Human Genetics. 103 (6): 1022–1029. doi:10.1016/j.ajhg.2018.10.023. PMC 6288405. PMID 30526861.
Long YS, Zhao QH, Su T, Cai YL, Zeng Y, Shi YW, et al. (November 2008). "Identification of the promoter region and the 5'-untranslated exons of the human voltage-gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5'-untranslated exons". Journal of Neuroscience Research. 86 (15): 3375–3381. doi:10.1002/jnr.21790. PMID 18655196. S2CID 33673297.
Goldin AL, Snutch T, Lübbert H, Dowsett A, Marshall J, Auld V, et al. (October 1986). "Messenger RNA coding for only the alpha subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes". Proceedings of the National Academy of Sciences of the United States of America. 83 (19): 7503–7507. Bibcode:1986PNAS...83.7503G. doi:10.1073/pnas.83.19.7503. PMC 386747. PMID 2429308.
George AL, Komisarof J, Kallen RG, Barchi RL (February 1992). "Primary structure of the adult human skeletal muscle voltage-dependent sodium channel". Annals of Neurology. 31 (2): 131–137. doi:10.1002/ana.410310203. PMID 1315496. S2CID 37892568.
Gellens ME, George AL, Chen LQ, Chahine M, Horn R, Barchi RL, et al. (January 1992). "Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel". Proceedings of the National Academy of Sciences of the United States of America. 89 (2): 554–558. Bibcode:1992PNAS...89..554G. doi:10.1073/pnas.89.2.554. PMC 48277. PMID 1309946.
Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, et al. (April 2000). "Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2". Nature Genetics. 24 (4): 343–345. doi:10.1038/74159. PMID 10742094.
Lossin C (February 2009). "A catalog of SCN1A variants". Brain & Development. 31 (2): 114–130. doi:10.1016/j.braindev.2008.07.011. PMID 18804930.
Fujiwara T, Sugawara T, Mazaki-Miyazaki E, Takahashi Y, Fukushima K, Watanabe M, et al. (March 2003). "Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures". Brain. 126 (Pt 3): 531–546. doi:10.1093/brain/awg053. PMID 12566275.
Ohmori I, Kahlig KM, Rhodes TH, Wang DW, George AL (October 2006). "Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy". Epilepsia. 47 (10): 1636–1642. doi:10.1111/j.1528-1167.2006.00643.x. PMID 17054685.
Kohrman DC, Smith MR, Goldin AL, Harris J, Meisler MH (October 1996). "A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting". The Journal of Neuroscience. 16 (19): 5993–5999. doi:10.1523/JNEUROSCI.16-19-05993.1996. PMC 6579185. PMID 8815882.
Bulman DE (1997). "Phenotype variation and newcomers in ion channel disorders". Human Molecular Genetics. 6 (10): 1679–1685. doi:10.1093/hmg/6.10.1679. PMID 9300659.
Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P (June 2001). "De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy". American Journal of Human Genetics. 68 (6): 1327–1332. doi:10.1086/320609. PMC 1226119. PMID 11359211.
Yu FH, Mantegazza M, Westenbroek RE, Robbins CA, Kalume F, Burton KA, et al. (September 2006). "Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy". Nature Neuroscience. 9 (9): 1142–1149. doi:10.1038/nn1754. PMID 16921370.
Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, et al. (April 2000). "Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2". Nature Genetics. 24 (4): 343–345. doi:10.1038/74159. PMID 10742094. S2CID 29543172.
Spampanato J, Escayg A, Meisler MH, Goldin AL (October 2001). "Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2". The Journal of Neuroscience. 21 (19): 7481–7490. doi:10.1523/jneurosci.21-19-07481.2001. PMC 6762922. PMID 11567038.
Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, et al. (June 2003). "Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy". Neurology. 60 (12): 1961–1967. doi:10.1212/01.wnl.0000069463.41870.2f. PMID 12821740. S2CID 604240.
Gee SH, Madhavan R, Levinson SR, Caldwell JH, Sealock R, Froehner SC (January 1998). "Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins". The Journal of Neuroscience. 18 (1): 128–137. doi:10.1523/jneurosci.18-01-00128.1998. PMC 6793384. PMID 9412493.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: SCN1A sodium channel, voltage-gated, type I, alpha subunit".
Meisler MH, O'Brien JE, Sharkey LM (June 2010). "Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects". The Journal of Physiology. 588 (Pt 11): 1841–1848. doi:10.1113/jphysiol.2010.188482. PMC 2901972. PMID 20351042.
Ogiwara I, Miyamoto H, Morita N, Atapour N, Mazaki E, Inoue I, et al. (May 2007). "Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation". The Journal of Neuroscience. 27 (22): 5903–5914. doi:10.1523/JNEUROSCI.5270-06.2007. PMC 6672241. PMID 17537961.
Tate SK, Depondt C, Sisodiya SM, Cavalleri GL, Schorge S, Soranzo N, et al. (April 2005). "Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin". Proceedings of the National Academy of Sciences of the United States of America. 102 (15): 5507–5512. Bibcode:2005PNAS..102.5507T. doi:10.1073/pnas.0407346102. PMC 556232. PMID 15805193.
Carvill GL, Engel KL, Ramamurthy A, Cochran JN, Roovers J, Stamberger H, et al. (December 2018). "Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies". American Journal of Human Genetics. 103 (6): 1022–1029. doi:10.1016/j.ajhg.2018.10.023. PMC 6288405. PMID 30526861.
Goldin AL, Snutch T, Lübbert H, Dowsett A, Marshall J, Auld V, et al. (October 1986). "Messenger RNA coding for only the alpha subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes". Proceedings of the National Academy of Sciences of the United States of America. 83 (19): 7503–7507. Bibcode:1986PNAS...83.7503G. doi:10.1073/pnas.83.19.7503. PMC 386747. PMID 2429308.
Gellens ME, George AL, Chen LQ, Chahine M, Horn R, Barchi RL, et al. (January 1992). "Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel". Proceedings of the National Academy of Sciences of the United States of America. 89 (2): 554–558. Bibcode:1992PNAS...89..554G. doi:10.1073/pnas.89.2.554. PMC 48277. PMID 1309946.
Kohrman DC, Smith MR, Goldin AL, Harris J, Meisler MH (October 1996). "A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting". The Journal of Neuroscience. 16 (19): 5993–5999. doi:10.1523/JNEUROSCI.16-19-05993.1996. PMC 6579185. PMID 8815882.
Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P (June 2001). "De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy". American Journal of Human Genetics. 68 (6): 1327–1332. doi:10.1086/320609. PMC 1226119. PMID 11359211.
Spampanato J, Escayg A, Meisler MH, Goldin AL (October 2001). "Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2". The Journal of Neuroscience. 21 (19): 7481–7490. doi:10.1523/jneurosci.21-19-07481.2001. PMC 6762922. PMID 11567038.
Gee SH, Madhavan R, Levinson SR, Caldwell JH, Sealock R, Froehner SC (January 1998). "Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins". The Journal of Neuroscience. 18 (1): 128–137. doi:10.1523/jneurosci.18-01-00128.1998. PMC 6793384. PMID 9412493.

scn1a.info (Global: low place; English: low place)

Lossin C. "SCN1A infobase". Archived from the original on 21 July 2011. Retrieved 30 October 2009. compilation of genetic variations in the SCN1A gene that alter the expression or function of Nav1.1

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Ito M, Nagafuji H, Okazawa H, Yamakawa K, Sugawara T, Mazaki-Miyazaki E, et al. (January 2002). "Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A". Epilepsy Research. 48 (1–2): 15–23. doi:10.1016/S0920-1211(01)00313-8. PMID 11823106. S2CID 25555020.
Catterall WA, Goldin AL, Waxman SG (December 2005). "International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels". Pharmacological Reviews. 57 (4): 397–409. doi:10.1124/pr.57.4.4. PMID 16382098. S2CID 7332624.
Long YS, Zhao QH, Su T, Cai YL, Zeng Y, Shi YW, et al. (November 2008). "Identification of the promoter region and the 5'-untranslated exons of the human voltage-gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5'-untranslated exons". Journal of Neuroscience Research. 86 (15): 3375–3381. doi:10.1002/jnr.21790. PMID 18655196. S2CID 33673297.
George AL, Komisarof J, Kallen RG, Barchi RL (February 1992). "Primary structure of the adult human skeletal muscle voltage-dependent sodium channel". Annals of Neurology. 31 (2): 131–137. doi:10.1002/ana.410310203. PMID 1315496. S2CID 37892568.
Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, et al. (April 2000). "Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2". Nature Genetics. 24 (4): 343–345. doi:10.1038/74159. PMID 10742094. S2CID 29543172.
Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, et al. (June 2003). "Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy". Neurology. 60 (12): 1961–1967. doi:10.1212/01.wnl.0000069463.41870.2f. PMID 12821740. S2CID 604240.

smh.com.au (Global: 132^nd place; English: 96^th place)

Robotham J (29 November 2008). "Sick babies denied treatment in DNA row –". National News. Sidney Morning Herald – smh.com.au. Retrieved 3 December 2008.

ua.ac.be (Global: low place; English: low place)

molgen.ua.ac.be

"The Variation Database of SCN1A". Department of Molecular Genetics. Vlaams Instituut voor Biotechnologie (VIB). Archived from the original on 7 October 2017.

web.archive.org (Global: 1^st place; English: 1^st place)

"The Variation Database of SCN1A". Department of Molecular Genetics. Vlaams Instituut voor Biotechnologie (VIB). Archived from the original on 7 October 2017.
Lossin C. "SCN1A infobase". Archived from the original on 21 July 2011. Retrieved 30 October 2009. compilation of genetic variations in the SCN1A gene that alter the expression or function of Nav1.1

SCN1A (English Wikipedia)

doi.org (Global: 2nd place; English: 2nd place)

ensembl.org (Global: 1,626th place; English: 1,007th place)

May2017.archive.ensembl.org

harvard.edu (Global: 18th place; English: 17th place)

ui.adsabs.harvard.edu

lovd.nl (Global: low place; English: low place)

databases.lovd.nl

nih.gov (Global: 4th place; English: 4th place)

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

scn1a.info (Global: low place; English: low place)

semanticscholar.org (Global: 11th place; English: 8th place)

api.semanticscholar.org

smh.com.au (Global: 132nd place; English: 96th place)

ua.ac.be (Global: low place; English: low place)

molgen.ua.ac.be

web.archive.org (Global: 1st place; English: 1st place)

doi.org (Global: 2^nd place; English: 2^nd place)

ensembl.org (Global: 1,626^th place; English: 1,007^th place)

harvard.edu (Global: 18^th place; English: 17^th place)

nih.gov (Global: 4^th place; English: 4^th place)

semanticscholar.org (Global: 11^th place; English: 8^th place)

smh.com.au (Global: 132^nd place; English: 96^th place)

web.archive.org (Global: 1^st place; English: 1^st place)