An LRP8 Variant Is Associated with Familial and Premature Coronary Artery Disease and Myocardial Infarction

Our previous genomewide linkage scan of 428 nuclear families (GeneQuest) identified a significant genetic susceptibility locus for premature myocardial infarction (MI) on chromosome 1p34-36. We analyzed candidate genes in the locus with a population-based association study involving probands with pr...

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Detalhes bibliográficos
Main Authors: Shen, Gong-Qing , Li, Lin , Girelli, Domenico , Seidelmann, Sara B. , Rao, Shaoqi , Fan, Chun , Park, Jeong Euy , Xi, Quansheng , Li, Jing , Hu, Ying , Olivieri, Oliviero , Marchant, Kandice , Barnard, John , Corrocher, Roberto , Elston, Robert , Cassano, June , Henderson, Susan , Hazen, Stanley L. , Plow, Edward F. , Topol, Eric J. , Wang, Qing K. 
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Human Genetics 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2227927/
https://ncbi.nlm.nih.gov/pubmed/17847002
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