Candidate gene association study of solute carrier family 11a members 1 (SLC11A1) and 2 (SLC11A2) genes in Alzheimer's disease

Neuroscience Letters

Volumn 374, Issue 2, 2005, Pages 124-128

  Jamieson, Sarra E ^a,b   White, Jacqueline K ^a,b   Howson, Joanna M M ^a,b   Pask, Rebecca ^a,b   Smith, Anne N ^a,b   Brayne, Carol ^c   Evans, John Grimley ^d   Xuereb, John ^e   Cairns, Nigel J ^f   Rubinsztein, David C ^a,b   Blackwell, Jenefer M ^a,b  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^c ADDENBROOKE S HOSPITAL   (United Kingdom)

^d UNIVERSITY OF OXFORD   (United Kingdom)

^e UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^f UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Alzheimer's disease; DCT1; DMT1; Genetic association; NRAMP1; Polymorphism

Indexed keywords

APOLIPOPROTEIN E; DIVALENT CATION; PROTON;

ALLELE; ALZHEIMER DISEASE; ARTICLE; CHROMOSOME 12; CHROMOSOME 2; CONTROLLED STUDY; ENDOSOME; FAMILY; FEMALE; GENDER; GENE EXPRESSION; GENETIC CODE; GENETIC VARIABILITY; HETEROZYGOTE DETECTION; HOMEOSTASIS; HUMAN; INFLAMMATION; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PLEIOTROPY; PRIORITY JOURNAL; RISK;

AGE OF ONSET; AGED; AGED, 80 AND OVER; ALZHEIMER DISEASE; APOLIPOPROTEINS E; CASE-CONTROL STUDIES; CATION TRANSPORT PROTEINS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; IRON-BINDING PROTEINS; MALE; ODDS RATIO; POLYMORPHISM, GENETIC; SEX FACTORS;

EID: 19944429951     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2004.10.038     Document Type: Article

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