COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese
Journal
Movement Disorders
Journal Volume
30
Journal Issue
3
Pages
436-437
ISSN
0885-3185
Date Issued
2015-03-01
Author(s)
SDGs
Other Subjects
cerebellum 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 Nucleotide
Publisher
John Wiley and Sons Inc.
Type
letter