A novel early onset phenotype in a zebrafish model of merosin deficient congenital muscular dystrophy

Merosin deficient congenital muscular dystrophy (MDC1A) is a severe neuromuscular disorder with onset in infancy that is associated with severe morbidities (particularly wheelchair dependence) and early mortality. It is caused by recessive mutations in the LAMA2 gene that encodes a subunit of the ex...

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Detalles Bibliográficos
Autores principales: Smith, Sarah J., Wang, Jeffrey C., Gupta, Vandana A., Dowling, James J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328290/
https://www.ncbi.nlm.nih.gov/pubmed/28241031
http://dx.doi.org/10.1371/journal.pone.0172648

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328290/
https://www.ncbi.nlm.nih.gov/pubmed/28241031
http://dx.doi.org/10.1371/journal.pone.0172648

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