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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Instituto Nacional Cardiovascular - INCOR
2021
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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 |