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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Bibliografiska uppgifter
I publikationen:Ann Neurol
Huvudupphovsmän: Lindqvist, Johan, Levy, Yotam, Pati‐Alam, Alisha, Hardeman, Edna C., Gregorevic, Paul, Ochala, Julien
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2016
Ämnen:
Research Articles
Länkar: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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