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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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| Publicado en: | Ann Neurol |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2016
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| Materias: | |
| Acceso en línea: | 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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