Modulating myosin restores muscle function in a mouse model of nemaline myopathy

OBJECTIVE: Nemaline myopathy, one of the most common congenital myopathies, is associated with mutations in various genes including ACTA1. This disease is also characterized by various forms/degrees of muscle weakness, with most cases being severe and resulting in death in infancy. Recent findings h...

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Detalhes bibliográficos
Publicado no:Ann Neurol
Main Authors: Lindqvist, Johan, Levy, Yotam, Pati‐Alam, Alisha, Hardeman, Edna C., Gregorevic, Paul, Ochala, Julien
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2016
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4950341/
https://ncbi.nlm.nih.gov/pubmed/26891371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24619
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