Articles with "bckdk stx1b" as a keyword



Association of three candidate genetic variants in ACMSD/TMEM163, GPNMB and BCKDK /STX1B with sporadic Parkinson’s disease in Han Chinese

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Published in 2019 at "Neuroscience Letters"

DOI: 10.1016/j.neulet.2019.03.019

Abstract: Large-scale meta-analyses of genome-wide association studies have identified that polymorphisms ACMSD/TMEM163 rs6430538, GPNMB rs199347 and BCKDK /STX1B rs14235 to be the risk loci for Parkinson's disease (PD) in a Caucasian population. However, the role of… read more here.

Keywords: gpnmb; acmsd tmem163; bckdk stx1b; han chinese ... See more keywords