Further evidence for role of a promoter variant in the TNFRSF6 gene in Alzheimer disease

Human Mutation

Volumn 21, Issue 1, 2003, Pages 53-60

  Feuk, Lars ^a   Prince, Jonathan A ^a   Blennow, Kaj ^b   Brookes, Anthony J ^a  

^a KAROLINSKA INSTITUTE   (Sweden)

^b SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

AD; Alzheimer; Association; FAS; Haplotype; Linkage disequilibrium; TNFRSF6

Indexed keywords

TUMOR NECROSIS FACTOR;

ADULT; ALZHEIMER DISEASE; ARTICLE; CHROMOSOME 10Q; COGNITION; CONTROLLED STUDY; DEMENTIA; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC LINKAGE; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MINI MENTAL STATE EXAMINATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROMOTER REGION; SINGLE NUCLEOTIDE POLYMORPHISM;

ALZHEIMER DISEASE; ANTIGENS, CD95; CASE-CONTROL STUDIES; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MOLECULAR SEQUENCE DATA; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS (GENETICS);

EID: 0037224318     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.10148     Document Type: Article

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