Single Nucleotide Polymorphisms in Multiple Novel Thrombospondin Genes May Be Associated With Familial Premature Myocardial Infarction | Zendy

Eric J. Topol | Zendy; Jeanette McCarthy | Zendy; Stacey B. Gabriel | Zendy; David J. Moliterno | Zendy; William J. Rogers | Zendy; L. Kristin Newby | Zendy; Matt Freedman | Zendy; Jennifer Metivier | Zendy; Ruth Cannata | Zendy; Christopher J. O’Donnell | Zendy; Kandice KottkeMarchant | Zendy; Gurunathan Murugesan | Zendy; Edward F. Plow | Zendy; Olga SteninaAdognravi | Zendy; George Q. Daley | Zendy

Open Access

Single Nucleotide Polymorphisms in Multiple Novel Thrombospondin Genes May Be Associated With Familial Premature Myocardial Infarction

Author(s) -

Eric J. Topol,

Jeanette McCarthy,

Stacey B. Gabriel,

David J. Moliterno,

William J. Rogers,

L. Kristin Newby,

Matt Freedman,

Jennifer Metivier,

Ruth Cannata,

Christopher J. O’Donnell,

Kandice KottkeMarchant,

Gurunathan Murugesan,

Edward F. Plow,

Olga SteninaAdognravi,

George Q. Daley

Publication year - 2001

Publication title -

circulation

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 7.795

H-Index - 607

eISSN - 1524-4539

pISSN - 0009-7322

DOI - 10.1161/hc4701.100910

Subject(s) - medicine , myocardial infarction , missense mutation , odds ratio , coronary artery disease , single nucleotide polymorphism , genetics , allele , cardiology , genotype , gene , biology , phenotype

Recent advances in high-throughput genomics technology have expanded our ability to catalogue allelic variants in large sets of candidate genes related to premature coronary artery disease.

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