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FAN1 modifies Huntington’s disease progression by stabilizing the expanded HTT CAG repeat
Huntington’s disease (HD) is an inherited neurodegenerative disease caused by an expanded CAG repeat in the huntingtin (HTT) gene. CAG repeat length explains around half of the variation in age at onset (AAO) but genetic variation elsewhere in the genome accounts for a significant proportion of the...
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| Pubblicato in: | Hum Mol Genet |
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| Autori principali: | , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6360275/ https://ncbi.nlm.nih.gov/pubmed/30358836 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy375 |
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