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Article

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy.

Journal of the American College of Cardiology - 18 Sept 2002

Feng Jinong, Yan Jin Yan, Buzin Carolyn H, Sommer Steve S, Towbin Jeffrey A

Abstract excerpt

OBJECTIVES: The goal of this study was to perform comprehensive mutation analysis of the dystrophin gene in patients with X-linked dilated cardiomyopathy (XLCM). BACKGROUND: X-linked dilated cardiomyopathy is a familial disease that is characterized by congestive heart failure without clinical signs of skeletal myopathy. Mutations in the dystrophin gene have been associated with the X-linked form of dilated...

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Share to Cardiomyopathy, Dilated
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Dystrophin

Share to Genetic Linkage

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Share to Polymorphism, Single-Stranded Conformational

Share to Promoter Regions, Genetic

Share to X Chromosome

Source

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PMID: 12354438
DOI: 10.1016/s0735-1097(02)02126-5

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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