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A rare case of familial restrictive cardiomyopathy, with mutations in MYH7 and ABCC9 genes
Restrictive cardiomyopathy is the least common type of cardiomyopathy, being defined by diastolic dysfunction and often unimpaired systolic function. Restrictive cardiomyopathies can be classified as familial or non-familial. Patients with familial restrictive cardiomyopathy can develop signs and sy...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Applied Systems srl
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086075/ https://www.ncbi.nlm.nih.gov/pubmed/32309617 http://dx.doi.org/10.15190/d.2019.12 |