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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 Non-Compaction.
Gehmlich K.
DOI
10.1161/CIRCGENETICS.116.001431
Type
Journal article
Publisher
American Heart Association
Publication Date
2016-09-20T00:00:00+00:00