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Dimerization is required for GARS-mediated neurotoxicity in dominant CMT disease
Charcot–Marie–Tooth (CMT) disease is a genetically heterogeneous group of peripheral neuropathies. Mutations in several aminoacyl-tRNA synthetase (ARS) genes have been implicated in inherited CMT disease. There are 12 reported CMT-causing mutations dispersed throughout the primary sequence of the hu...
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| Publicado no: | Hum Mol Genet |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4805310/ https://ncbi.nlm.nih.gov/pubmed/27008886 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw031 |
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