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pro vyhledávání: '"Mohammad Mahdi Mortazavipour"'
MYBPC3Δ25bp intronic deletion in hypertrophic cardiomyopathy patients and healthy Iranian population
Autor:
Leila Emrahi, Shirin Shahbazi, Mehrnoush Toufan Tabrizi, Mohammad Mahdi Mortazavipour, Mir Ali Seyyedi
Publikováno v:
مجله پزشکی دانشگاه علوم پزشکی تبریز, Vol 43, Iss 1, Pp 22-28 (2021)
Background: Hypertrophic cardiomyopathy is a common genetic cardiovascular disease with autosomal dominant inheritance and MYBPC3 gene has been frequently linked to its pathogenesis. Since, carriers of the 25 nucleotides deletion located on intron 32
Externí odkaz:
https://doaj.org/article/c4bf32ff6f774d2a9e1e0c028413e261
MYBPC3Δ25bp intronic deletion in hypertrophic cardiomyopathy patients and healthy Iranian population
Autor:
Mohammad Mahdi Mortazavipour, Mir Ali Seyyedi, Leila Emrahi, Mehrnoush Toufan Tabrizi, Shirin Shahbazi
Publikováno v:
Medical Journal of Tabriz University of Medical Sciences and Health Services. 43:22-28
Background: Hypertrophic cardiomyopathy is a common genetic cardiovascular disease with autosomal dominant inheritance and MYBPC3 gene has been frequently linked to its pathogenesis. Since, carriers of the 25 nucleotides deletion located on intron 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4261861298df6c9f8a2ad0813a631c7d
https://doi.org/10.34172/mj.2021.023
https://doi.org/10.34172/mj.2021.023