Hypertonia-linked protein Trak1 functions with mitofusins to promote mitochondrial tethering and fusion
ABSTRACT 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, e...
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| Principais autores: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2017-09-01
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| Series: | Protein & Cell |
| Assuntos: | |
| Acceso en liña: | http://link.springer.com/article/10.1007/s13238-017-0469-4 |
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