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Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease. (2016)

First Author: Muggenthaler M

Attributed to: Genetic modifiers of hypertrophic cardiomyopathy in the Old Order Amish funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ijcard.2016.02.082

PubMed Identifier: 26922712

Publication URI: http://europepmc.org/abstract/MED/26922712

Type: Journal Article/Review

Volume: 210

Parent Publication: International journal of cardiology

ISSN: 0167-5273