Lieb, Wolfgang ; Zeller, Tanja ; Mangino, Massimo ; Götz, Anika ; Braund, Peter ; Wenzel, Juergen J. 
; Horn, Christian ; Proust, Carole ; Linsel-Nitschke, Patrick ; Amouyel, Philippe ; Bruse, Petra ; Arveiler, Dominique ; König, Inke R. ; Ferrières, Jean ; Ziegler, Andreas ; Balmforth, Anthony J. ; Evans, Alun ; Ducimetière, Pierre ; Cambien, Francois ; Hengstenberg, Christian ; Stark, Klaus ; Hall, Alistair S. ; Schunkert, Heribert ; Blankenberg, Stefan ; Samani, Nilesh J. ; Erdmann, Jeanette ; Tiret, Laurence
; Horn, Christian ; Proust, Carole ; Linsel-Nitschke, Patrick ; Amouyel, Philippe ; Bruse, Petra ; Arveiler, Dominique ; König, Inke R. ; Ferrières, Jean ; Ziegler, Andreas ; Balmforth, Anthony J. ; Evans, Alun ; Ducimetière, Pierre ; Cambien, Francois ; Hengstenberg, Christian ; Stark, Klaus ; Hall, Alistair S. ; Schunkert, Heribert ; Blankenberg, Stefan ; Samani, Nilesh J. ; Erdmann, Jeanette ; Tiret, Laurence 
Zusammenfassung
Coronary artery disease (CAD) and myocardial infarction (MI) have a genetic basis, but the precise genetic underpinning remains controversial. Recently, an association of the LRP8 R952Q polymorphism (rs5174) with familial premature CAD/MI was reported. We analysed rs5174 (or the perfect proxy rs5177) in 1,210 patients with familial MI and 1,015 controls from the German MI Family study, in 1,926 ...
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