Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease

Human Mutation

Volumn 28, Issue 11, 2007, Pages 1065-1073

  Liang, Xueying ^a,b   Martin, Eden R ^c,e   Schnetz Boutaud, Nathalie ^a,b   Bartlett, Jackie ^a,b   Anderson, Brent ^a,b   Züchner, Stephan ^c,e   Gwirtsman, Harry ^d   Schmechel, Don ^c   Carney, Regina ^c   Gilbert, John R ^c,e   Pericak Vance, Margaret A ^c,e   Haines, Jonathan L ^a,b  

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d VETERANS AFFAIRS MEDICAL CENTER   (United States)

^e UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

Alpha catenin; Alzheimer disease; APOE; Association; Chromosome 10; IDE; Linkage; LRRTM3; PLAU; TNFRSF6; VR22

Indexed keywords

ALPHA CATENIN; APOLIPOPROTEIN E;

ALZHEIMER DISEASE; ARTICLE; CASE CONTROL STUDY; CHROMOSOME 10; CONTROLLED STUDY; GENE; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENOTYPE; HUMAN; IDE GENE; LINKAGE ANALYSIS; LRRTM3 GENE; MAJOR CLINICAL STUDY; ONSET AGE; PLAU GENE; PRIORITY JOURNAL; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS; TNFRSF6 GENE; VR22 GENE;

AGE OF ONSET; AGED; ALZHEIMER DISEASE; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 10; GENETIC HETEROGENEITY; HUMANS; LINKAGE (GENETICS); POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 35648975571     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20567     Document Type: Article

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