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Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locus

Background: In recent years, non-syndromic idiopathic cardiomyopathies have increasingly been characterised as autosomal dominant conditions caused by single gene mutations. Loci have been identified for hypertrophic and dilated cardiomyopathy, and in some cases the same loci are associated with res...

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Bibliografiske detaljer
Main Authors: Zhang, J, Kumar, A, Kaplan, L, Fricker, F, Wallace, M
Format: Artigo
Sprog:English
Udgivet: BMJ Group 2005
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1736124/
https://ncbi.nlm.nih.gov/pubmed/16061566
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.030189
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