Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/17200
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dc.contributor.authorAlfakih, K-
dc.contributor.authorBrown, B-
dc.contributor.authorLawrance, RA-
dc.contributor.authorWarburton, P-
dc.contributor.authorMaqbool, A-
dc.contributor.authorWalters, K-
dc.contributor.authorSamani, NJ-
dc.contributor.authorBall, SG-
dc.contributor.authorBalmforth, AJ-
dc.contributor.authorHall, AS-
dc.date.accessioned2012-10-24T09:03:12Z-
dc.date.available2012-10-24T09:03:12Z-
dc.date.issued2007-11-
dc.identifier.citationATHEROSCLEROSIS, 2007, 195 (1), pp. e32-e38-
dc.identifier.urihttp://hdl.handle.net/2381/17200-
dc.description.abstractTo assess the association of the angiotensin II type 2 (AT2) receptor (-1332 G/A) gene polymorphism with premature coronary artery disease (CAD) and investigate for a further role in both myocardial infarction and predominantly stenotic atherosclerosis requiring revascularisation.-
dc.formatmetadata-
dc.language.isoeng-
dc.sourcePubMed-
dc.source.urihttp://www.ncbi.nlm.nih.gov/pubmed/-
dc.subjectAged-
dc.subjectAtherosclerosis-
dc.subjectChromosomes-
dc.subjectHuman-
dc.subjectX-
dc.subjectConstriction-
dc.subjectPathologic-
dc.subjectFamily Health-
dc.subjectFemale-
dc.subjectGenetic Predisposition to Disease-
dc.subjectGenotype-
dc.subjectHumans-
dc.subjectMale-
dc.subjectMiddle Aged-
dc.subjectMyocardial Infarction-
dc.subjectNeovascularization-
dc.subjectPathologic-
dc.subjectPolymorphism-
dc.subjectGenetic-
dc.subjectReceptor-
dc.subjectAngiotensin-
dc.subjectType 2-
dc.titleEffect of a common X-linked angiotensin II type 2-receptor gene polymorphism (-1332 G/A) on the occurrence of premature myocardial infarction and stenotic atherosclerosis requiring revascularization.-
dc.typeJournal Article-
dc.identifier.doi10.1016/j.atherosclerosis.2007.01.028-
dc.identifier.eissn1879-1484-
dc.identifier.piiS0021-9150(07)00074-3-
dc.description.irispid20636-
Appears in Collections:Published Articles, Dept. of Cardiovascular Sciences

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