Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy

Neurobiology of Aging

Volumn 36, Issue 2, 2015, Pages 1222.e7-1222.e11

  Chen, Yong Ping ^a   Zhao, Bi ^a   Cao, Bei ^a   Song, Wei ^a   Guo, XiaoYan ^a   Wei, Qian Qian ^a   Yang, Yuan ^a   Yuan, Li Xing ^b   Shang, Hui Fang ^a  

^a SICHUAN UNIVERSITY   (China)

^b SICHUAN UNIVERSITY   (China)

Author keywords

COQ2; Multiple system atrophy; Mutation; Val393Ala; Variant

Indexed keywords

ALANINE; VALINE; 4-HYDROXYBENZOATE POLYPRENYLTRANSFERASE; TRANSFERASE;

ADULT; ARTICLE; CHINESE; CONTROLLED STUDY; COQ2 GENE; DNA SEQUENCE; ETHNICITY; EXON; FEMALE; GENE; GENE FREQUENCY; GENE LOCATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; SEQUENCE ANALYSIS; SHY DRAGER SYNDROME; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; GENETICS; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PROCEDURES; RISK;

AGED; ALKYL AND ARYL TRANSFERASES; ASIAN CONTINENTAL ANCESTRY GROUP; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HUMANS; MALE; MIDDLE AGED; MULTIPLE SYSTEM ATROPHY; MUTATION; RISK;

EID: 84922937095     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2014.09.010     Document Type: Article

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