Frequency and Phenotypes of Familial Dilated Cardiomyopathy

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death

A Jervell, F Lange-Nielsen · American Heart Journal · 1957 · 1.6K citations

Heart Failure, Pediatrics, Sudden Death +6

Defective myosin VIIA gene responsible for Usher syndrome type IB

Dominique Well, Stéphane Blanchard, Josseline Kaplan et al. · Nature · 1995 · 1.1K citations

Mendelian Disorder, Genetic Disorder, Genetics +3

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

Virginia V. Michels, Patricia P. Moll, Fletcher A. Miller et al. · New England Journal of Medicine · 1992 · 703 citations · Full text

A type VII myosin encoded by the mouse deafness gene shaker-1

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Knockout Mouse, Molecular Physiology, Genetic Disorder +8

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

Jeffrey A. Towbin, J. Fielding Hejtmancik, Paul A. Brink et al. · Circulation · 1993 · 515 citations · Full text