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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Detalles Bibliográficos
Autores principales: Tian, Lei, Ding, Sheng, You, Yun, Li, Tong-ruei, Liu, Yan, Wu, Xiaohui, Sun, Ling, Xu, Tian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2015
Materias:
Resource Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4457035/
https://www.ncbi.nlm.nih.gov/pubmed/26035871
http://dx.doi.org/10.1242/dmm.019430

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4457035/
https://www.ncbi.nlm.nih.gov/pubmed/26035871
http://dx.doi.org/10.1242/dmm.019430

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