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Article

Isolation of a de novo mutant myocardial beta MHC protein in a pedigree with hypertrophic cardiomyopathy.

Human molecular genetics - 1 Nov 1994

Greve G, Bachinski L, Friedman D L, Czernuzewicz G, Anan R, Towbin J, Seidman C E, Roberts R

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

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PMID: 7874131

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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.

Related research

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Research trail→

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Isolation of a de novo mutant myocardial beta MHC protein in a pedigree with hypertrophic cardiomyopathy.PMID 7874131Read ↗

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A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.Semantic proximity Read ↗

The cardiac myosin heavy chain Arg-403-->Gln mutation that causes hypertrophic cardiomyopathy does not affect the actin- or ATP-binding capacities of two size-limited recombinant myosin heavy chain fragments.Semantic proximity Read ↗

Missense mutation of the beta-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy.Semantic proximity Read ↗

Novel mutation in the alpha-tropomyosin gene and transition from hypertrophic to hypocontractile dilated cardiomyopathy.Semantic proximity Read ↗

Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.Semantic proximity Read ↗

A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy.Semantic proximity Read ↗

Functional analysis of the mutations in the human cardiac beta-myosin that are responsible for familial hypertrophic cardiomyopathy. Implication for the clinical outcome.Semantic proximity Read ↗

Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.Semantic proximity Read ↗

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