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...

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Detalles Bibliográficos
Autores principales: Bonaventura, Jiri, Polakova, Eva, Vejtasova, Veronika, Veselka, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
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

Internet

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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