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A modifier of Huntington's disease onset at the MLH1 locus
Huntington's disease (HD) is a dominantly inherited neurodegenerative disease caused by an expanded CAG repeat in HTT. Many clinical characteristics of HD such as age at motor onset are determined largely by the size of HTT CAG repeat. However, emerging evidence strongly supports a role for oth...
Gardado en:
| Publicado en: | Hum Mol Genet |
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| Main Authors: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6455020/ https://ncbi.nlm.nih.gov/pubmed/28934397 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx286 |
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