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Volumn 629, Issue , 2016, Pages 160-164

Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson's disease and increase susceptibility to dementia in a Flanders-Belgian cohort

Author keywords

GBA; Genotype phenotype correlation; Glucocerebrosidase; Parkinson's disease

Indexed keywords

ADULT; AGED; ARTICLE; BELGIAN; CONTROLLED STUDY; DEMENTIA; EXON; FEMALE; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE PHENOTYPE CORRELATION; GLUCOSYLCERAMIDASE GENE; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PARKINSON DISEASE; PRIORITY JOURNAL; RATING SCALE; RISK FACTOR; SCORING SYSTEM; SEQUENCE ANALYSIS; BELGIUM; COHORT ANALYSIS; COMPLICATION; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; HETEROZYGOTE; MIDDLE AGED; MUTATION; PHENOTYPE; SEVERITY OF ILLNESS INDEX;

EID: 84978252668     PISSN: 03043940     EISSN: 18727972     Source Type: Journal    
DOI: 10.1016/j.neulet.2016.07.008     Document Type: Article
Times cited : (22)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.