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Dynamin 2 (DNM2) as Cause of, and Modifier for, Human Neuromuscular Disease
Dynamin 2 (DNM2) belongs to a family of large GTPases that are well known for mediating membrane fission by oligomerizing at the neck of membrane invaginations. Autosomal dominant mutations in the ubiquitously expressed DNM2 cause 2 discrete neuromuscular diseases: autosomal dominant centronuclear m...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer International Publishing
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277281/ https://www.ncbi.nlm.nih.gov/pubmed/30426359 http://dx.doi.org/10.1007/s13311-018-00686-0 |