CHIN-HSIEN LINTan E.-K.CHIH-CHAO YANGYi Z.RUEY-MEEI WU2020-11-032020-11-032015-03-010885-3185https://www.scopus.com/inward/record.uri?eid=2-s2.0-84924545322&doi=10.1002%2fmds.26138&partnerID=40&md5=ed53d58943c486d4cde732a05a63fa3chttps://scholars.lib.ntu.edu.tw/handle/123456789/520048[SDGs]SDG3cerebellum disease; Chinese; controlled study; coq2 gene; gene; gene frequency; genetic association; genetic code; genetic susceptibility; genetic variability; heterozygote; human; Letter; major clinical study; Parkinson disease; phenotype; priority journal; rare disease; Shy Drager syndrome; Asian continental ancestry group; cerebellum; female; genetics; genotype; male; odds ratio; pathology; Shy Drager syndrome; single nucleotide polymorphism; 4-hydroxybenzoate polyprenyltransferase; transferase; Alkyl and Aryl Transferases; Asian Continental Ancestry Group; Cerebellum; Female; Gene Frequency; Genotype; Humans; Male; Multiple System Atrophy; Odds Ratio; Polymorphism, Single Nucleotideletter10.1002/mds.26138255945032-s2.0-84924545322