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Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

Title: Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Authors: Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
Contributors: Ehret, Georg Benedikt
Source: ISSN: 0028-4793 ; New England Journal of Medicine, vol. 374, no. 12 (2016) p. 1134-1144.
Publication Year: 2016
Collection: Université de Genève: Archive ouverte UNIGE
Subject Terms: info:eu-repo/classification/ddc/616; Aged; Angiopoietin-like 4 Protein; Angiopoietins/genetics; Cell Adhesion Molecules/genetics; Coronary Artery Disease/genetics; Female; Genotyping Techniques; Humans; Lipoprotein Lipase/antagonists & inhibitors/genetics/metabolism; Male; Middle Aged; Mutation; Missense; Risk Factors; Sequence Analysis; DNA; Triglycerides/blood/genetics
Description: The discovery of low-frequency coding variants affecting the risk of coronary artery disease has facilitated the identification of therapeutic targets.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/26934567; unige:127757
Availability: https://archive-ouverte.unige.ch/unige:127757
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.CB6B3923
Database: BASE