Congenital muscular dystrophy (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Congenital muscular dystrophy" in English language version.

refsWebsite

Global rank English rank

27nih.gov

4^th place

18web.archive.org

1^st place

11doi.org

2^nd place

11omim.org

4,380^th place

4,305^th place

7worldcat.org

5^th place

2semanticscholar.org

11^th place

8^th place

1medscape.com

719^th place

636^th place

1aan.com

low place

1nmd-journal.com

low place

1sciencedirect.com

149^th place

178^th place

aan.com

"Congenital muscular dystrophy". Guidelines American Academy of Neurology. 2015. Archived from the original on 19 October 2020. Retrieved 28 April 2016.

doi.org

Bertini, Enrico; D'Amico, Adele; Gualandi, Francesca; Petrini, Stefania (2011-12-01). "Congenital Muscular Dystrophies: A Brief Review". Seminars in Pediatric Neurology. 18 (4): 277–288. doi:10.1016/j.spen.2011.10.010. ISSN 1071-9091. PMC 3332154. PMID 22172424.
El-Sobky, Tamer A.; Abdulhady, Hala; Mahmoud, Shady; Amen, John (31 January 2024). "Orthopedic manifestations of congenital muscular dystrophy subtypes in children: Emerging signatures need consolidation: a scoping review". Journal of Musculoskeletal Surgery and Research. 8: 11–23. doi:10.25259/JMSR_229_2023.
Zambon, Alberto A.; Muntoni, Francesco (2021-10-01). "Congenital muscular dystrophies: What is new?". Neuromuscular Disorders. 31 (10): 931–942. doi:10.1016/j.nmd.2021.07.009. ISSN 0960-8966. PMID 34470717. S2CID 236462260.
Kirschner, Janbernd (2013-01-01), Dulac, Olivier; Lassonde, Maryse; Sarnat, Harvey B. (eds.), "Chapter 143 - Congenital muscular dystrophies", Handbook of Clinical Neurology, Pediatric Neurology Part III, 113, Elsevier: 1377–1385, doi:10.1016/b978-0-444-59565-2.00008-3, ISBN 9780444595652, PMID 23622361, archived from the original on 2023-10-04, retrieved 2022-05-11
Jimenez-Mallebrera, C.; Brown, S. C.; Sewry, C. A.; Muntoni, F. (2005-04-01). "Congenital muscular dystrophy: molecular and cellular aspects". Cellular and Molecular Life Sciences. 62 (7): 809–823. doi:10.1007/s00018-004-4510-4. ISSN 1420-9071. PMID 15868406. S2CID 24662420.
Bönnemann, Carsten G. (July 2011). "The collagen VI-related myopathies: muscle meets its matrix". Nature Reviews Neurology. 7 (7): 379–390. doi:10.1038/nrneurol.2011.81. ISSN 1759-4766. PMC 5210181. PMID 21691338.
Fu, Xiao-Na; Xiong, Hui (2017-11-05). "Genetic and Clinical Advances of Congenital Muscular Dystrophy". Chinese Medical Journal. 130 (21): 2624–2631. doi:10.4103/0366-6999.217091. ISSN 0366-6999. PMC 5678264. PMID 29067961.
Martin, Paul T (2006). "Mechanisms of Disease: congenital muscular dystrophies—glycosylation takes center stage". Nature Clinical Practice Neurology. 2 (4): 222–230. doi:10.1038/ncpneuro0155. ISSN 1745-834X. PMC 2855642. PMID 16932553.
Bădilă, E; Lungu, II; Grumezescu, AM; Scafa Udriște, A (12 May 2021). "Diagnosis of Cardiac Abnormalities in Muscular Dystrophies". Medicina (Kaunas, Lithuania). 57 (5): 488. doi:10.3390/medicina57050488. PMC 8151418. PMID 34066119.
Finsterer, J; Ramaciotti, C; Wang, CH; Wahbi, K; Rosenthal, D; Duboc, D; Melacini, P (September 2010). "Cardiac findings in congenital muscular dystrophies". Pediatrics. 126 (3): 538–45. doi:10.1542/peds.2010-0208. PMID 20679303.
Bönnemann, Carsten G.; Wang, Ching H.; Quijano-Roy, Susana; Deconinck, Nicolas; Bertini, Enrico; Ferreiro, Ana; Muntoni, Francesco; Sewry, Caroline; Béroud, Christophe; Mathews, Katherine D.; Moore, Steven A.; Bellini, Jonathan; Rutkowski, Anne; North, Kathryn N. (1 April 2014). "Diagnostic approach to the congenital muscular dystrophies". Neuromuscular Disorders. 24 (4): 289–311. doi:10.1016/j.nmd.2013.12.011. PMC 5258110. PMID 24581957.

medscape.com

emedicine.medscape.com

"Congenital Muscular Dystrophy Workup: Laboratory Studies, Imaging Studies, Other Tests". emedicine.medscape.com. Archived from the original on 2021-01-19. Retrieved 2016-04-28.

nih.gov

pubmed.ncbi.nlm.nih.gov

Sparks, Susan; Quijano-Roy, Susana; Harper, Amy; Rutkowski, Anne; Gordon, Erynn; Hoffman, Eric P.; Pegoraro, Elena (1993-01-01). "Congenital Muscular Dystrophy Overview – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Congenital Muscular Dystrophy Overview. Seattle (WA): University of Washington, Seattle. PMID 20301468. Archived from the original on 2020-08-04. Retrieved 2017-08-30.update 2012
Bertini, Enrico; D'Amico, Adele; Gualandi, Francesca; Petrini, Stefania (2011-12-01). "Congenital Muscular Dystrophies: A Brief Review". Seminars in Pediatric Neurology. 18 (4): 277–288. doi:10.1016/j.spen.2011.10.010. ISSN 1071-9091. PMC 3332154. PMID 22172424.
Astrea, Guja; Battini, Roberta; Lenzi, Sara; Frosini, Silvia; Bonetti, Silvia; Moretti, Elena; Perazza, Silvia; Santorelli, Filippo M.; Pecini, Chiara (October 2016). "Learning disabilities in neuromuscular disorders: a springboard for adult life". Acta Myologica. 35 (2): 90–95. ISSN 1128-2460. PMC 5343745. PMID 28344438.
Zambon, Alberto A.; Muntoni, Francesco (2021-10-01). "Congenital muscular dystrophies: What is new?". Neuromuscular Disorders. 31 (10): 931–942. doi:10.1016/j.nmd.2021.07.009. ISSN 0960-8966. PMID 34470717. S2CID 236462260.
Kirschner, Janbernd (2013-01-01), Dulac, Olivier; Lassonde, Maryse; Sarnat, Harvey B. (eds.), "Chapter 143 - Congenital muscular dystrophies", Handbook of Clinical Neurology, Pediatric Neurology Part III, 113, Elsevier: 1377–1385, doi:10.1016/b978-0-444-59565-2.00008-3, ISBN 9780444595652, PMID 23622361, archived from the original on 2023-10-04, retrieved 2022-05-11
Saito, Kayoko (1993). "Fukuyama Congenital Muscular Dystrophy". GeneReviews®. University of Washington, Seattle. PMID 20301385. Archived from the original on 2019-09-18. Retrieved 2023-10-04.
Jimenez-Mallebrera, C.; Brown, S. C.; Sewry, C. A.; Muntoni, F. (2005-04-01). "Congenital muscular dystrophy: molecular and cellular aspects". Cellular and Molecular Life Sciences. 62 (7): 809–823. doi:10.1007/s00018-004-4510-4. ISSN 1420-9071. PMID 15868406. S2CID 24662420.
Bönnemann, Carsten G. (July 2011). "The collagen VI-related myopathies: muscle meets its matrix". Nature Reviews Neurology. 7 (7): 379–390. doi:10.1038/nrneurol.2011.81. ISSN 1759-4766. PMC 5210181. PMID 21691338.
Fu, Xiao-Na; Xiong, Hui (2017-11-05). "Genetic and Clinical Advances of Congenital Muscular Dystrophy". Chinese Medical Journal. 130 (21): 2624–2631. doi:10.4103/0366-6999.217091. ISSN 0366-6999. PMC 5678264. PMID 29067961.
Martin, Paul T (2006). "Mechanisms of Disease: congenital muscular dystrophies—glycosylation takes center stage". Nature Clinical Practice Neurology. 2 (4): 222–230. doi:10.1038/ncpneuro0155. ISSN 1745-834X. PMC 2855642. PMID 16932553.
Bădilă, E; Lungu, II; Grumezescu, AM; Scafa Udriște, A (12 May 2021). "Diagnosis of Cardiac Abnormalities in Muscular Dystrophies". Medicina (Kaunas, Lithuania). 57 (5): 488. doi:10.3390/medicina57050488. PMC 8151418. PMID 34066119.
Finsterer, J; Ramaciotti, C; Wang, CH; Wahbi, K; Rosenthal, D; Duboc, D; Melacini, P (September 2010). "Cardiac findings in congenital muscular dystrophies". Pediatrics. 126 (3): 538–45. doi:10.1542/peds.2010-0208. PMID 20679303.
Quijano-Roy, Susana; Sparks, Susan; Rutkowski, Anne (1993-01-01). "LAMA2 Muscular Dystrophy". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). LAMA2-Related Muscular Dystrophy. Seattle (WA): University of Washington, Seattle. PMID 22675738.update 2012
Bönnemann, Carsten G.; Wang, Ching H.; Quijano-Roy, Susana; Deconinck, Nicolas; Bertini, Enrico; Ferreiro, Ana; Muntoni, Francesco; Sewry, Caroline; Béroud, Christophe; Mathews, Katherine D.; Moore, Steven A.; Bellini, Jonathan; Rutkowski, Anne; North, Kathryn N. (1 April 2014). "Diagnostic approach to the congenital muscular dystrophies". Neuromuscular Disorders. 24 (4): 289–311. doi:10.1016/j.nmd.2013.12.011. PMC 5258110. PMID 24581957.

ncbi.nlm.nih.gov

Sparks, Susan; Quijano-Roy, Susana; Harper, Amy; Rutkowski, Anne; Gordon, Erynn; Hoffman, Eric P.; Pegoraro, Elena (1993-01-01). "Congenital Muscular Dystrophy Overview – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Congenital Muscular Dystrophy Overview. Seattle (WA): University of Washington, Seattle. PMID 20301468. Archived from the original on 2020-08-04. Retrieved 2017-08-30.update 2012
Bertini, Enrico; D'Amico, Adele; Gualandi, Francesca; Petrini, Stefania (2011-12-01). "Congenital Muscular Dystrophies: A Brief Review". Seminars in Pediatric Neurology. 18 (4): 277–288. doi:10.1016/j.spen.2011.10.010. ISSN 1071-9091. PMC 3332154. PMID 22172424.
Astrea, Guja; Battini, Roberta; Lenzi, Sara; Frosini, Silvia; Bonetti, Silvia; Moretti, Elena; Perazza, Silvia; Santorelli, Filippo M.; Pecini, Chiara (October 2016). "Learning disabilities in neuromuscular disorders: a springboard for adult life". Acta Myologica. 35 (2): 90–95. ISSN 1128-2460. PMC 5343745. PMID 28344438.
Saito, Kayoko (1993). "Fukuyama Congenital Muscular Dystrophy". GeneReviews®. University of Washington, Seattle. PMID 20301385. Archived from the original on 2019-09-18. Retrieved 2023-10-04.
Bönnemann, Carsten G. (July 2011). "The collagen VI-related myopathies: muscle meets its matrix". Nature Reviews Neurology. 7 (7): 379–390. doi:10.1038/nrneurol.2011.81. ISSN 1759-4766. PMC 5210181. PMID 21691338.
Fu, Xiao-Na; Xiong, Hui (2017-11-05). "Genetic and Clinical Advances of Congenital Muscular Dystrophy". Chinese Medical Journal. 130 (21): 2624–2631. doi:10.4103/0366-6999.217091. ISSN 0366-6999. PMC 5678264. PMID 29067961.
Martin, Paul T (2006). "Mechanisms of Disease: congenital muscular dystrophies—glycosylation takes center stage". Nature Clinical Practice Neurology. 2 (4): 222–230. doi:10.1038/ncpneuro0155. ISSN 1745-834X. PMC 2855642. PMID 16932553.
Bădilă, E; Lungu, II; Grumezescu, AM; Scafa Udriște, A (12 May 2021). "Diagnosis of Cardiac Abnormalities in Muscular Dystrophies". Medicina (Kaunas, Lithuania). 57 (5): 488. doi:10.3390/medicina57050488. PMC 8151418. PMID 34066119.
Quijano-Roy, Susana; Sparks, Susan; Rutkowski, Anne (1993-01-01). "LAMA2 Muscular Dystrophy". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). LAMA2-Related Muscular Dystrophy. Seattle (WA): University of Washington, Seattle. PMID 22675738.update 2012
Bönnemann, Carsten G.; Wang, Ching H.; Quijano-Roy, Susana; Deconinck, Nicolas; Bertini, Enrico; Ferreiro, Ana; Muntoni, Francesco; Sewry, Caroline; Béroud, Christophe; Mathews, Katherine D.; Moore, Steven A.; Bellini, Jonathan; Rutkowski, Anne; North, Kathryn N. (1 April 2014). "Diagnostic approach to the congenital muscular dystrophies". Neuromuscular Disorders. 24 (4): 289–311. doi:10.1016/j.nmd.2013.12.011. PMC 5258110. PMID 24581957.

ghr.nlm.nih.gov

Reference, Genetics Home. "Walker-Warburg syndrome". Genetics Home Reference. Archived from the original on 2018-07-28. Retrieved 2016-04-26.
Reference, Genetics Home. "Fukuyama congenital muscular dystrophy". Genetics Home Reference. Archived from the original on 2016-05-13. Retrieved 2016-04-26.

nlm.nih.gov

"Hypotonia: MedlinePlus Medical Encyclopedia". www.nlm.nih.gov. Archived from the original on 2016-07-05. Retrieved 2016-04-28.

nmd-journal.com

Zambon, Alberto A.; Muntoni, Francesco (2021-10-01). "Congenital muscular dystrophies: What is new?". Neuromuscular Disorders. 31 (10): 931–942. doi:10.1016/j.nmd.2021.07.009. ISSN 0960-8966. PMID 34470717. S2CID 236462260.

omim.org

"OMIM Entry - # 253280 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3". www.omim.org. Archived from the original on 2015-12-11. Retrieved 2016-04-26.
"Error 403".
"OMIM Entry - # 612937 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Io; CDG1O". www.omim.org. Archived from the original on 2019-06-08. Retrieved 2016-04-26.
"OMIM Entry - # 615042 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U". www.omim.org. Archived from the original on 2019-06-23. Retrieved 2016-04-26.
"OMIM Entry - # 608799 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie; CDG1E". www.omim.org. Archived from the original on 2019-09-29. Retrieved 2016-04-26.
"OMIM Entry - # 602771 - RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1". www.omim.org. Archived from the original on 2015-12-07. Retrieved 2016-04-26.
"OMIM Entry - # 613205 - MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED". www.omim.org. Archived from the original on 2019-09-18. Retrieved 2016-04-26.
"OMIM Entry - # 613204 - MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY". www.omim.org. Archived from the original on 2021-12-15. Retrieved 2016-04-26.
"OMIM Entry - # 607855 - MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A". www.omim.org. Archived from the original on 2020-04-14. Retrieved 2016-04-26.
"OMIM Entry - % 609456 - MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE". www.omim.org. Archived from the original on 2021-12-15. Retrieved 2016-04-26.
"OMIM Entry - # 254090 - ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1; UCMD1". omim.org. Archived from the original on 2015-12-24. Retrieved 2016-04-26.

sciencedirect.com

Kirschner, Janbernd (2013-01-01), Dulac, Olivier; Lassonde, Maryse; Sarnat, Harvey B. (eds.), "Chapter 143 - Congenital muscular dystrophies", Handbook of Clinical Neurology, Pediatric Neurology Part III, 113, Elsevier: 1377–1385, doi:10.1016/b978-0-444-59565-2.00008-3, ISBN 9780444595652, PMID 23622361, archived from the original on 2023-10-04, retrieved 2022-05-11

semanticscholar.org

api.semanticscholar.org

Zambon, Alberto A.; Muntoni, Francesco (2021-10-01). "Congenital muscular dystrophies: What is new?". Neuromuscular Disorders. 31 (10): 931–942. doi:10.1016/j.nmd.2021.07.009. ISSN 0960-8966. PMID 34470717. S2CID 236462260.
Jimenez-Mallebrera, C.; Brown, S. C.; Sewry, C. A.; Muntoni, F. (2005-04-01). "Congenital muscular dystrophy: molecular and cellular aspects". Cellular and Molecular Life Sciences. 62 (7): 809–823. doi:10.1007/s00018-004-4510-4. ISSN 1420-9071. PMID 15868406. S2CID 24662420.

web.archive.org

Sparks, Susan; Quijano-Roy, Susana; Harper, Amy; Rutkowski, Anne; Gordon, Erynn; Hoffman, Eric P.; Pegoraro, Elena (1993-01-01). "Congenital Muscular Dystrophy Overview – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Congenital Muscular Dystrophy Overview. Seattle (WA): University of Washington, Seattle. PMID 20301468. Archived from the original on 2020-08-04. Retrieved 2017-08-30.update 2012
"Congenital Muscular Dystrophy Workup: Laboratory Studies, Imaging Studies, Other Tests". emedicine.medscape.com. Archived from the original on 2021-01-19. Retrieved 2016-04-28.
"Congenital muscular dystrophy". Guidelines American Academy of Neurology. 2015. Archived from the original on 19 October 2020. Retrieved 28 April 2016.
"Hypotonia: MedlinePlus Medical Encyclopedia". www.nlm.nih.gov. Archived from the original on 2016-07-05. Retrieved 2016-04-28.
Kirschner, Janbernd (2013-01-01), Dulac, Olivier; Lassonde, Maryse; Sarnat, Harvey B. (eds.), "Chapter 143 - Congenital muscular dystrophies", Handbook of Clinical Neurology, Pediatric Neurology Part III, 113, Elsevier: 1377–1385, doi:10.1016/b978-0-444-59565-2.00008-3, ISBN 9780444595652, PMID 23622361, archived from the original on 2023-10-04, retrieved 2022-05-11
Saito, Kayoko (1993). "Fukuyama Congenital Muscular Dystrophy". GeneReviews®. University of Washington, Seattle. PMID 20301385. Archived from the original on 2019-09-18. Retrieved 2023-10-04.
"OMIM Entry - # 253280 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3". www.omim.org. Archived from the original on 2015-12-11. Retrieved 2016-04-26.
Reference, Genetics Home. "Walker-Warburg syndrome". Genetics Home Reference. Archived from the original on 2018-07-28. Retrieved 2016-04-26.
"OMIM Entry - # 612937 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Io; CDG1O". www.omim.org. Archived from the original on 2019-06-08. Retrieved 2016-04-26.
"OMIM Entry - # 615042 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U". www.omim.org. Archived from the original on 2019-06-23. Retrieved 2016-04-26.
"OMIM Entry - # 608799 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie; CDG1E". www.omim.org. Archived from the original on 2019-09-29. Retrieved 2016-04-26.
"OMIM Entry - # 602771 - RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1". www.omim.org. Archived from the original on 2015-12-07. Retrieved 2016-04-26.
"OMIM Entry - # 613205 - MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED". www.omim.org. Archived from the original on 2019-09-18. Retrieved 2016-04-26.
"OMIM Entry - # 613204 - MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY". www.omim.org. Archived from the original on 2021-12-15. Retrieved 2016-04-26.
Reference, Genetics Home. "Fukuyama congenital muscular dystrophy". Genetics Home Reference. Archived from the original on 2016-05-13. Retrieved 2016-04-26.
"OMIM Entry - # 607855 - MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A". www.omim.org. Archived from the original on 2020-04-14. Retrieved 2016-04-26.
"OMIM Entry - % 609456 - MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE". www.omim.org. Archived from the original on 2021-12-15. Retrieved 2016-04-26.
"OMIM Entry - # 254090 - ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1; UCMD1". omim.org. Archived from the original on 2015-12-24. Retrieved 2016-04-26.

worldcat.org

search.worldcat.org

Bertini, Enrico; D'Amico, Adele; Gualandi, Francesca; Petrini, Stefania (2011-12-01). "Congenital Muscular Dystrophies: A Brief Review". Seminars in Pediatric Neurology. 18 (4): 277–288. doi:10.1016/j.spen.2011.10.010. ISSN 1071-9091. PMC 3332154. PMID 22172424.
Astrea, Guja; Battini, Roberta; Lenzi, Sara; Frosini, Silvia; Bonetti, Silvia; Moretti, Elena; Perazza, Silvia; Santorelli, Filippo M.; Pecini, Chiara (October 2016). "Learning disabilities in neuromuscular disorders: a springboard for adult life". Acta Myologica. 35 (2): 90–95. ISSN 1128-2460. PMC 5343745. PMID 28344438.
Zambon, Alberto A.; Muntoni, Francesco (2021-10-01). "Congenital muscular dystrophies: What is new?". Neuromuscular Disorders. 31 (10): 931–942. doi:10.1016/j.nmd.2021.07.009. ISSN 0960-8966. PMID 34470717. S2CID 236462260.
Jimenez-Mallebrera, C.; Brown, S. C.; Sewry, C. A.; Muntoni, F. (2005-04-01). "Congenital muscular dystrophy: molecular and cellular aspects". Cellular and Molecular Life Sciences. 62 (7): 809–823. doi:10.1007/s00018-004-4510-4. ISSN 1420-9071. PMID 15868406. S2CID 24662420.
Bönnemann, Carsten G. (July 2011). "The collagen VI-related myopathies: muscle meets its matrix". Nature Reviews Neurology. 7 (7): 379–390. doi:10.1038/nrneurol.2011.81. ISSN 1759-4766. PMC 5210181. PMID 21691338.
Fu, Xiao-Na; Xiong, Hui (2017-11-05). "Genetic and Clinical Advances of Congenital Muscular Dystrophy". Chinese Medical Journal. 130 (21): 2624–2631. doi:10.4103/0366-6999.217091. ISSN 0366-6999. PMC 5678264. PMID 29067961.
Martin, Paul T (2006). "Mechanisms of Disease: congenital muscular dystrophies—glycosylation takes center stage". Nature Clinical Practice Neurology. 2 (4): 222–230. doi:10.1038/ncpneuro0155. ISSN 1745-834X. PMC 2855642. PMID 16932553.