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Miocardiopatía hipertrófica septal, la gran simuladora

Hypertrophic cardiomyopathy is the more commonly (60 to 70 percent) genetically determined disease of the heart muscle caused by mutations in one of several sarcomere genes that encode components of the heart’s contractile apparatus. It is characterized by disproportionate hypertrophy in the absence...

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Detalles Bibliográficos
Autores principales: Forero, Santiago, Moreno, Nelson Leandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Nacional Cardiovascular - INCOR 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506570/
https://www.ncbi.nlm.nih.gov/pubmed/37727664
http://dx.doi.org/10.47487/apcyccv.v2i4.171