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MUTANT HUNTINGTIN AND MITOCHONDRIAL DYSFUNCTION
Huntington's disease (HD) is a fatal inherited neurodegenerative disorder that gradually robs affected individuals of memory, cognitive skills, and normal movements. While research has identified a single faulty gene, the huntingtin gene, as the cause of the disease, a cure remains elusive. Str...
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| Huvudupphovsmän: | , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2008
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2613540/ https://ncbi.nlm.nih.gov/pubmed/18951640 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tins.2008.09.004 |
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