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...

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Detalles Bibliográficos
Publicado en:Hum Mol Genet
Main Authors: Lee, Jong-Min, Chao, Michael J., Harold, Denise, Abu Elneel, Kawther, Gillis, Tammy, Holmans, Peter, Jones, Lesley, Orth, Michael, Myers, Richard H., Kwak, Seung, Wheeler, Vanessa C., MacDonald, Marcy E., Gusella, James F.
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2017
Assuntos:
Association Studies Articles
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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