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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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| 出版年: | J Struct Biol |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Academic Press
2016
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| 主題: | |
| オンライン･アクセス: | 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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