Llwytho...
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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | J Struct Biol |
|---|---|
| Prif Awduron: | , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Academic Press
2016
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| Pynciau: | |
| Mynediad Ar-lein: | 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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