Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. (2014)

First Author: Lange LA

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2014.01.010

PubMed Identifier: 24507775

Publication URI: http://europepmc.org/abstract/MED/24507775

Type: Journal Article/Review

Volume: 94

Parent Publication: American journal of human genetics

Issue: 2

ISSN: 0002-9297