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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Bibliografski detalji
Izdano u:PLoS One
Glavni autori: 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.
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2018
Teme:
Research Article
Online pristup: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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