Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32

Dilated cardiomyopathy, characterized by ventricular dilatation and decreased systolic contraction, is twofold to threefold more common as a cause of heart failure than hypertrophic cardiomyopathy and costs several billion dollars annually. The idiopathic form occurring early in life, with a 75% mor...

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Veröffentlicht in:	Circulation (New York, N.Y.) N.Y.), 1995-12, Vol.92 (12), p.3387-3389
Hauptverfasser:	DURAND, J.-B, BACHINSKI, L. L, BRUGADA, R, DAIGER, S, GREGORITCH, J. M, ANDERSON, J. L, QUINONES, M, TOWBIN, J. A, ROBERTS, R, BIELING, L. C, CZERNUSZEWICZ, G. Z, ABCHEE, A. B, QUN TAO YU, TAPSCOTT, T, HILL, R, IFEGWU, J, MARIAN, A. J
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Biological and medical sciences Cardiology. Vascular system Cardiomyopathy, Dilated - diagnostic imaging Cardiomyopathy, Dilated - genetics Child Chromosome Mapping Chromosomes, Human, Pair 1 Female Genetic Linkage Heart Humans Male Medical sciences Middle Aged Myocarditis. Cardiomyopathies Pedigree Polymerase Chain Reaction Ultrasonography
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