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Article

MYBPC3 in hypertrophic cardiomyopathy: from mutation identification to RNA-based correction

11 Dec 2013

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 24337823
DOI: 10.1007/s00424-013-1409-7

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MYBPC3 in hypertrophic cardiomyopathy: from mutation identification to RNA-based correctionPMID 24337823Read ↗

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Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.Semantic proximity Read ↗

An Update on MYBPC3 Gene Mutation in Hypertrophic Cardiomyopathy.Semantic proximity Read ↗

Reanalysis of Next-generation Sequencing Data in Patients With Hypertrophic Cardiomyopathy: Contribution of Spliceogenic MYBPC3 Variants in an Italian Cohort.Semantic proximity Read ↗

Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

Targeting the population for gene therapy with MYBPC3.Semantic proximity Read ↗

From malignant mutations to malignant domains: the continuing search for prognostic significance in the mutant genes causing hypertrophic cardiomyopathySemantic proximity Read ↗

Hypertrophic cardiomyopathy. Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategySemantic proximity Read ↗

Genetics of hypertrophic cardiomyopathy: A review of current state.Semantic proximity Read ↗

Protein haploinsufficiency drivers identify MYBPC3 variants that cause hypertrophic cardiomyopathy.Semantic proximity Read ↗

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