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Leiomodin-3-deficient mice display nemaline myopathy with fast-myofiber atrophy
Nemaline myopathy (NM) is one of the most common forms of congenital myopathy, and affects either fast myofibers, slow myofibers, or both. However, an animal model for congenital myopathy with fast-myofiber-specific atrophy is not available. Furthermore, mutations in the leiomodin-3 (LMOD3) gene hav...
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| Publicado no: | Dis Model Mech |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4457035/ https://ncbi.nlm.nih.gov/pubmed/26035871 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.019430 |
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