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Publikováno v:
Investigacion clinica. 55(1)
Hypertrophic cardiomyopathy (HCM) is a cardiac disease, characterized by marked hypertrophy and genetic variability. HCM has been associated with sarcomere protein mutations, being cardiac beta-myosin (coded by the MYH7 gene) and myosin binding prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3ca24a477951f7135513156da14e0e89
https://pubmed.ncbi.nlm.nih.gov/24758099
https://pubmed.ncbi.nlm.nih.gov/24758099
