Abstract
Background Small human genetic studies have variably linked single nucleotide polymorphisms (SNPs) in chemokine receptor genes to cardiometabolic disease.
- Title
- COMMON OR RARE GENETIC VARIATION IN THE CHEMOKINE RECEPTORS CCR2, CCR5, AND CX3CR1 DOES NOT RELATE TO CORONARY HEART DISEASE OR MYOCARDIAL INFARCTION IN HUMANS
- Creators - without role
- Jessica Golbus - Hospital of the University of PennsylvaniaNathan Stitziel - Hospital of the University of PennsylvaniaNilesh Samani - Hospital of the University of PennsylvaniaJeanette Erdmann - Hospital of the University of PennsylvaniaHeribert Schunkert - Hospital of the University of PennsylvaniaPanos Deloukas - Hospital of the University of PennsylvaniaDanish Saleheen - Hospital of the University of PennsylvaniaMartin Farrall - Hospital of the University of PennsylvaniaRuth McPherson - Hospital of the University of PennsylvaniaHugh Watkins - Hospital of the University of PennsylvaniaSekar Kathiresan - Hospital of the University of PennsylvaniaMuredach Reilly - Hospital of the University of Pennsylvania
- Publication Details
- Journal of the American College of Cardiology, Vol.67(13), pp.1891-1891
- Publisher
- Elsevier Limited
- Identifiers
- 9935604208331
- Academic Unit
- King Abdulaziz University
- Language
- English
- Resource Type
- Journal article