Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate

American Journal of Human Genetics

Volumn 89, Issue 1, 2011, Pages 131-138

  Kullo, Iftikhar J ^a   Ding, Keyue ^a   Shameer, Khader ^a   McCarty, Catherine A ^b   Jarvik, Gail P ^c   Denny, Joshua C ^d   Ritchie, Marylyn D ^e   Ye, Zi ^a   Crosslin, David R ^c   Chisholm, Rex L ^f   Manolio, Teri A ^g   Chute, Christopher G ^a  

^a MAYO CLINIC   (United States)

^b MARSHFIELD CLINIC   (United States)

^c UNIVERSITY OF WASHINGTON   (United States)

^d VANDERBILT UNIVERSITY   (United States)

^e VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f NORTHWESTERN UNIVERSITY   (United States)

^g NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C3B RECEPTOR;

ADULT; AGED; ARTICLE; ELECTRONIC MEDICAL RECORD; ERYTHROCYTE SEDIMENTATION RATE; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 80051550030     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2011.05.019     Document Type: Article

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