Localization of a Gene Responsible for Familial Dilated Cardiomyopathy to Chromosome 1q32
- 15 December 1995
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation
- Vol. 92 (12) , 3387-3389
- https://doi.org/10.1161/01.cir.92.12.3387
Abstract
Background Dilated cardiomyopathy, characterized by ventricular dilatation and decreased systolic contraction, is twofold to threefold more common as a cause of heart failure than hypertrophic card...Keywords
This publication has 6 references indexed in Scilit:
- A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1Nature Genetics, 1994
- Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute Workshop)The American Journal of Cardiology, 1992
- An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular DystrophyScience, 1992
- The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated CardiomyopathyNew England Journal of Medicine, 1992
- A simple salting out procedure for extracting DNA from human nucleated cellsNucleic Acids Research, 1988
- A routine method for the establishment of permanent growing lymphoblastoid cell linesHuman Genetics, 1986