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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

Attributed to: Multiparametric advanced fluorescence imaging strategies for in situ analysis of live cell signalling funded by MRC

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

Parent Publication: Circulation: Cardiovascular Genetics

Issue: 5

ISSN: 1942-3268