A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort

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作者
Patrick Weydt
Selma M Soyal
G Bernhard Landwehrmeyer
Wolfgang Patsch
机构
[1] Neurology,Laboratory Medicine
[2] Ulm University,undefined
[3] Paracelsus Medical University,undefined
[4] Pharmacology,undefined
[5] Paracelsus Medical University,undefined
来源
BMC Neurology | / 14卷
关键词
Genetic modifier; Gender effect; Neurodegeneration; Huntington disease;
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