Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction

Circulation

Volumn 104, Issue 22, 2001, Pages 2641-2644

  Topol, Eric J ^a   McCarthy, Jeanette ^f   Gabriel, Stacey ^b   Moliterno, David J ^a   Rogers, William J ^d   Newby, L Kristin ^e   Freedman, Matt ^b   Metivier, Jennifer ^f   Cannata, Ruth ^a   O'Donnell, Christopher J ^c   Kottke Marchant, Kandice ^a   Murugesan, Gurunathan ^a   Plow, Edward F ^a   Stenina, Olga ^a   Daley, George Q ^b  

^a LERNER RESEARCH INSTITUTE   (United States)

^b WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH   (United States)

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

^d UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^e DUKE UNIVERSITY MEDICAL CENTER   (United States)

^f MILLENNIUM PHARMACEUTICALS INC   (United States)

Author keywords

Atherosclerosis; Coronary disease; Genes; Genetics; Myocardial infarction

Indexed keywords

BIOCHEMICAL MARKER; THROMBOSPONDIN;

ADULT; AGED; ARTICLE; ENDOTHELIUM CELL; EXTRACELLULAR MATRIX; FAMILIAL DISEASE; FEMALE; GENETIC ASSOCIATION; GENETIC VARIABILITY; HEART INFARCTION; HIGH RISK POPULATION; HUMAN; LONGEVITY; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROTEIN FAMILY; REVASCULARIZATION; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 0035960593     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/hc4701.100910     Document Type: Article

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