Natural disease history of the dy(2J) mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy

Merosin deficient congenital muscular dystrophy 1A (MDC1A) is a very rare autosomal recessive disorder caused by mutations in the LAMA2 gene leading to severe and progressive muscle weakness and atrophy. Although over 350 causative mutations have been identified for MDC1A, no treatment is yet availa...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Pasteuning-Vuhman, S., Putker, K., Tanganyika-de Winter, C. L., Boertje-van der Meulen, J. W., van Vliet, L., Overzier, M., Plomp, J. J., Aartsma-Rus, A., van Putten, M.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2018
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5953480/
https://ncbi.nlm.nih.gov/pubmed/29763467
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0197388
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