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Failure to identify modifiers of NEBULIN-related nemaline myopathy in two pre-clinical models of the disease
Nemaline myopathy is a rare neuromuscular disorder that affects 1 in 50,000 live births, with prevalence as high as 1 in 20,000 in certain populations. 13 genes have been linked to nemaline myopathy (NM), all of which are associated with the thin filament of the muscle sarcomere. Of the 13 associate...
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| Publicado no: | Biol Open |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists Ltd
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6777365/ https://ncbi.nlm.nih.gov/pubmed/31530540 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/bio.044867 |
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