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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...
Uloženo v:
| Vydáno v: | Biol Open |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Company of Biologists Ltd
2019
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| Témata: | |
| On-line přístup: | 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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