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Hypertonia-linked protein Trak1 functions with mitofusins to promote mitochondrial tethering and fusion
Hypertonia is a neurological dysfunction associated with a number of central nervous system disorders, including cerebral palsy, Parkinson’s disease, dystonia, and epilepsy. Genetic studies have identified a homozygous truncation mutation in Trak1 that causes hypertonia in mice. Moreover, elevated T...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Higher Education Press
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053349/ https://www.ncbi.nlm.nih.gov/pubmed/28924745 http://dx.doi.org/10.1007/s13238-017-0469-4 |