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Genetic Testing in Patients with Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is a common inherited heart disease with an estimated prevalence of up to 1 in 200 individuals. In the majority of cases, HCM is considered a Mendelian disease, with mainly autosomal dominant inheritance. Most pathogenic variants are usually detected in genes for sa...
Autores principales: | Bonaventura, Jiri, Polakova, Eva, Vejtasova, Veronika, Veselka, Josef |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509044/ https://www.ncbi.nlm.nih.gov/pubmed/34638741 http://dx.doi.org/10.3390/ijms221910401 |
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