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Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model
Dynamin 2 (DNM2) is a key protein of the endocytosis and intracellular membrane trafficking machinery. Mutations in the DNM2 gene cause autosomal dominant centronuclear myopathy (CNM) and a knock-in mouse model expressing the most frequent human DNM2 mutation in CNM (Knock In-Dnm2(R465W/+)) develops...
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| Publicado en: | Sci Rep |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Nature Publishing Group UK
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6367339/ https://ncbi.nlm.nih.gov/pubmed/30733559 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-38184-0 |
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