Sindrome di Dejerine-Sottas (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrome di Dejerine-Sottas" in Italian language version.

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doi.org

dx.doi.org

Hayasaka K, Himoro M, Sawaishi Y, et al., De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III), in Nat. Genet., vol. 5, n. 3, novembre 1993, pp. 266-8, DOI:10.1038/ng1193-266, PMID 7506095.
Roa BB, Dyck PJ, Marks HG, Chance PF, Lupski JR, Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene, in Nat. Genet., vol. 5, n. 3, novembre 1993, pp. 269-73, DOI:10.1038/ng1193-269, PMID 8275092.
Kabzinska D, Drac H, Sherman DL, et al., Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene, in Neurology, vol. 66, n. 5, marzo 2006, pp. 745-7, DOI:10.1212/01.wnl.0000201269.46071.35, PMID 16534116.
Boerkoel CF, Takashima H, Bacino CA, Daentl D, Lupski JR, EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy ^{[collegamento interrotto]}, in Neurogenetics, vol. 3, n. 3, luglio 2001, pp. 153-7, DOI:10.1007/s100480100107, PMID 11523566.

neurology.org

Kabzinska D, Drac H, Sherman DL, et al., Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene, in Neurology, vol. 66, n. 5, marzo 2006, pp. 745-7, DOI:10.1212/01.wnl.0000201269.46071.35, PMID 16534116.

nih.gov

ncbi.nlm.nih.gov

Hayasaka K, Himoro M, Sawaishi Y, et al., De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III), in Nat. Genet., vol. 5, n. 3, novembre 1993, pp. 266-8, DOI:10.1038/ng1193-266, PMID 7506095.
Roa BB, Dyck PJ, Marks HG, Chance PF, Lupski JR, Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene, in Nat. Genet., vol. 5, n. 3, novembre 1993, pp. 269-73, DOI:10.1038/ng1193-269, PMID 8275092.
Kabzinska D, Drac H, Sherman DL, et al., Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene, in Neurology, vol. 66, n. 5, marzo 2006, pp. 745-7, DOI:10.1212/01.wnl.0000201269.46071.35, PMID 16534116.
Boerkoel CF, Takashima H, Bacino CA, Daentl D, Lupski JR, EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy ^{[collegamento interrotto]}, in Neurogenetics, vol. 3, n. 3, luglio 2001, pp. 153-7, DOI:10.1007/s100480100107, PMID 11523566.

oadoi.org

Hayasaka K, Himoro M, Sawaishi Y, et al., De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III), in Nat. Genet., vol. 5, n. 3, novembre 1993, pp. 266-8, DOI:10.1038/ng1193-266, PMID 7506095.
Roa BB, Dyck PJ, Marks HG, Chance PF, Lupski JR, Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene, in Nat. Genet., vol. 5, n. 3, novembre 1993, pp. 269-73, DOI:10.1038/ng1193-269, PMID 8275092.

springer.de

link.springer.de

Boerkoel CF, Takashima H, Bacino CA, Daentl D, Lupski JR, EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy ^{[collegamento interrotto]}, in Neurogenetics, vol. 3, n. 3, luglio 2001, pp. 153-7, DOI:10.1007/s100480100107, PMID 11523566.