Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
Abstract
Huntington's disease is caused by a CAG repeat expansion in the huntingtin gene, HTT. Age at onset has been used as a quantitative phenotype in genetic analysis looking for Huntington's disease modifiers, but is hard to define and not always available. Therefore, we aimed to generate a novel measure of disease progression and to identify genetic markers associated with this progression measure.We generated a progression score on the basis of...
Paper Details
Title
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
Published Date
Sep 1, 2017
Journal
Volume
16
Issue
9
Pages
701 - 711
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