| Literature DB >> 7951328 |
S Kass1, C MacRae, H L Graber, E A Sparks, D McNamara, H Boudoulas, C T Basson, P B Baker, R J Cody, M C Fishman.
Abstract
Longitudinal evaluation of a seven generation kindred with an inherited conduction system defect and dilated cardiomyopathy demonstrated autosomal dominant transmission of a progressive disorder that both perturbs atrioventricular conduction and depresses cardiac contractility. To elucidate the molecular genetic basis for this disorder, a genome-wide linkage analysis was performed. Polymorphic loci near the centromere of chromosome 1 demonstrated linkage to the disease locus (maximum multipoint lod score = 13.2 in the interval between D1S305 and D1S176). Based on the disease phenotype and map location we speculate that gap junction protein connexin 40 is a candidate for mutations that result in conduction system disease and dilated cardiomyopathy.Entities:
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Year: 1994 PMID: 7951328 DOI: 10.1038/ng0894-546
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330