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Mutation-Specific Effects on Thin Filament Length in Thin Filament Myopathy
OBJECTIVE: Thin filament myopathies are among the most common nondystrophic congenital muscular disorders, and are caused by mutations in genes encoding proteins that are associated with the skeletal muscle thin filament. Mechanisms underlying muscle weakness are poorly understood, but might involve...
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Publicado no: | Ann Neurol |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2016
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4911820/ https://ncbi.nlm.nih.gov/pubmed/27074222 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24654 |
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