A modifier of Huntington's disease onset at the MLH1 locus
Abstract
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 other genetic factors in modifying the disease pathogenesis driven by mutant huntingtin. A recent genome-wide association analysis to discover genetic...
Paper Details
Title
A modifier of Huntington's disease onset at the MLH1 locus
Published Date
Jul 21, 2017
Journal
Volume
26
Issue
19
Pages
3859 - 3867
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