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...

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Detalles Bibliográficos
Autores principales: Neagoe, Oana, Ciobanu, Anda, Diaconu, Rodica, Mirea, Oana, Donoiu, Ionuț, Militaru, Constantin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Applied Systems srl 2019
Materias:
Original Article
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

Internet

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

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