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Structural insights into the centronuclear myopathy-associated functions of BIN1 and dynamin 2
Centronuclear myopathies (CNMs) are genetic diseases whose symptoms are muscle weakness and atrophy (wasting) and centralised nuclei. Recent human genetic studies have isolated several groups of mutations. Among them, many are found in two interacting proteins essential to clathrin-mediated endocyto...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Academic Press
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039012/ https://www.ncbi.nlm.nih.gov/pubmed/27343996 http://dx.doi.org/10.1016/j.jsb.2016.06.015 |