Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease

Parkinsonism and Related Disorders

Volumn 18, Issue 5, 2012, Pages 638-640

  Zhang, Yu ^a   Chen, Shuai ^a   Xiao, Qin ^a   Cao, Li ^a   Liu, Jun ^a   Rong, Tian Yi ^a   Ma, Jian Fang ^a   Wang, Gang ^a   Wang, Ying ^a   Chen, Sheng Di ^a,b  

^a SHANGHAI SECOND MEDICAL UNIVERSITY   (China)

^b SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

Chinese; Mutation; Parkinson's disease; VPS35

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHINA; CHINESE; CONTROLLED STUDY; ETHNICITY; EXON; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; HUMAN; MAJOR CLINICAL STUDY; MALE; PARKINSON DISEASE; PRIORITY JOURNAL; VACUOLAR PROTEIN SORTING 35 GENE;

ADULT; AGED; AGED, 80 AND OVER; ASPARAGINE; ASPARTIC ACID; CHINA; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MUTATION; PARKINSON DISEASE; VESICULAR TRANSPORT PROTEINS;

EID: 84862776825     PISSN: 13538020     EISSN: 18735126     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2012.02.011     Document Type: Article

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