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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發表在: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.
格式: Artigo
語言:Inglês
出版: Oxford University Press 2017
主題:
Association Studies Articles
在線閱讀: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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