Chasing the molecular background of hypertrophic cardiomyopathy: The continuing saga to predict adverse outcomes with sarcomere mutations
Author:
Funder
Ministry of Health of the Czech Republic
Publisher
Elsevier BV
Reference14 articles.
1. Genetic testing in patients with hypertrophic cardiomyopathy;Bonaventura;Int. J. Mol. Sci.,2021
2. Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives;Maron;J. Am. Coll. Cardiol.,2012
3. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy;Watkins;N. Engl. J. Med.,1992
4. Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield;Thomson;Genet. Med.,2019
5. Clinical exome sequencing unravels the diverse spectrum of genetic heterogeneity and genotype-phenotype correlations in hypertrophic cardiomyopathy;Harikrishnan;Int. J. Cardiol.,2024
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