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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...
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| Publicado no: | J Struct Biol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Academic Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5039012/ https://ncbi.nlm.nih.gov/pubmed/27343996 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jsb.2016.06.015 |
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