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)
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
Volume: 9
Parent Publication: Circulation. Cardiovascular genetics
Issue: 5
ISSN: 1942-3268