Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction. (2016)

First Author: Hastings R

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1161/circgenetics.116.001431

PubMed Identifier: 27625337

Publication URI: http://europepmc.org/abstract/MED/27625337

Type: Journal Article/Review

Volume: 9

Parent Publication: Circulation. Cardiovascular genetics

Issue: 5

ISSN: 1942-3268