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

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