SCOPUS 정보 검색 플랫폼

Volumn 86, Issue 10, 2008, Pages 1163-1170

Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction

(27) Lieb, Wolfgang a Zeller, Tanja b Mangino, Massimo c Götz, Anika a Braund, Peter c Wenzel, Juergen J b Horn, Christian a Proust, Carole d,e Linsel Nitschke, Patrick a Amouyel, Philippe d Bruse, Petra a Arveiler, Dominique f König, Inke R a Ferrières, Jean d Ziegler, Andreas a Balmforth, Anthony J i Evans, Alun g Ducimetière, Pierre d Cambien, Francois d,e Hengstenberg, Christian h more..

a UNIVERSITY OF LÜBECK (Germany)

b JOHANNES GUTENBERG UNIVERSITY (Germany)

c UNIVERSITY OF LEICESTER (United Kingdom)

d INSERM (France)

e SORBONNE UNIVERSITÉ (France)

f UNIVERSITÉ DE STRASBOURG (France)

g QUEEN'S UNIVERSITY BELFAST (United Kingdom)

h UNIVERSITY HOSPITAL REGENSBURG (Germany)

i UNIVERSITY OF LEEDS (United Kingdom)

Author keywords

Coronary artery disease; Genetics; LRP8; Myocardial infarction; Polymorphism

Indexed keywords

ADULT; AGED; ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; FAMILIAL HEART INFARCTION; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HEART INFARCTION; HUMAN; LRP8 GENE; MAJOR CLINICAL STUDY; MALE; MATRICARIA; POPULATION RESEARCH; PROSPECTIVE STUDY; SINGLE NUCLEOTIDE POLYMORPHISM; SPORADIC HEART INFARCTION;

EID: 52549088057 PISSN: 09462716 EISSN: None Source Type: Journal
DOI: 10.1007/s00109-008-0376-5 Document Type: Article

Times cited : (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.