Absence of association on aldehyde dehydrogenase 2 (ALDH2) polymorphism with Mongolian Alzheimer patients

Neuroscience Letters

Volumn 468, Issue 3, 2010, Pages 312-315

  Zhou, Sirui ^a,c   Huriletemuer, ^b,d   Wang, Jing ^a,c   zhang, Chunyu ^d   Zhao, Shigang ^d   Wang, De Sheng ^b   Wang, Binbin ^a,c   Ma, Xu ^c,e  

^a GRADUATE SCHOOL OF PEKING UNION MEDICAL COLLEGE   (China)

^b HARBIN MEDICAL UNIVERSITY   (China)

^c NATIONAL RESEARCH INSTITUTE FOR FAMILY PLANNING   (China)

^d INNER MONGOLIA MEDICAL COLLEGE   (China)

^e WORLD HEALTH ORGANIZATION   (Switzerland)

Author keywords

Alzheimer's disease; Apolipoprotein E; Association analysis; Mitochondrial aldehyde dehydrogenase; Mongolian

Indexed keywords

ALDEHYDE DEHYDROGENASE ISOENZYME 2; APOLIPOPROTEIN E4;

ADULT; AGED; ALZHEIMER DISEASE; ARTICLE; CHINESE; CONTROLLED STUDY; DNA POLYMORPHISM; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC DIFFERENCE; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RISK FACTOR;

AGED; AGED, 80 AND OVER; ALDEHYDE DEHYDROGENASE; ALZHEIMER DISEASE; ASIAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MONGOLIA; POLYMORPHISM, GENETIC; RISK FACTORS;

EID: 72249101513     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2009.11.022     Document Type: Article

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