An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction

American Journal of Human Genetics

Volumn 81, Issue 4, 2007, Pages 780-791

  Shen, Gong Qing ^a,b   Li, Lin ^a   Girelli, Domenico ^e   Seidelmann, Sara B ^a,b   Rao, Shaoqi ^a   Fan, Chun ^a,b   Jeong, Euy Park ^f   Xi, Quansheng ^a,b   Li, Jing ^c   Hu, Ying ^a,b   Olivieri, Oliviero ^e   Marchant, Kandice ^a   Barnard, John ^a   Corrocher, Roberto ^e   Elston, Robert ^d   Cassano, June ^a,b   Henderson, Susan ^a,b   Hazen, Stanley L ^a   Plow, Edward F ^a,b   Topol, Eric J ^g   Wang, Qing K ^a,b   more..

^a LERNER RESEARCH INSTITUTE   (United States)

^b CLEVELAND CLINIC LERNER COLLEGE OF MEDICINE   (United States)

^c Case Western Reserve University   (United States)

^d CASE WESTERN RESERVE UNIVERSITY   (United States)

^e UNIVERSITY OF VERONA   (Italy)

^f Sungkyunkwan University   (South Korea)

^g SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOGEN ACTIVATED PROTEIN KINASE P38; OXIDIZED LOW DENSITY LIPOPROTEIN;

ADULT; ANGIOCARDIOGRAPHY; ARTICLE; CONTROLLED STUDY; CORONARY ARTERY DISEASE; ENZYME ACTIVATION; FEMALE; FOLLOW UP; GENE LOCUS; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HEART INFARCTION; HUMAN; LRP8 GENE; MAJOR CLINICAL STUDY; MALE; MUTATOR GENE; PRIORITY JOURNAL;

EID: 35349013508     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/521581     Document Type: Article

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