Open AccessHypertrophic cardiomyopathy caused by mutations in the <I>PRKAG2</I> gene
Author(s) -
I. V. Leontyeva,
Natalia Shcherbakova,
Е П Калачанова,
S. A. Thermosesov,
В. С. Сухоруков
Publication year - 2022
Publication title -
rossijskij vestnik perinatologii i pediatrii
Language(s) - English
Resource type - Journals
eISSN - 2500-2228
pISSN - 1027-4065
DOI - 10.21508/1027-4065-2022-67-4-99-107
Subject(s) - medicine , cardiology , hypertrophic cardiomyopathy , muscle hypertrophy , cardiomyopathy , heart failure , sudden cardiac death , sudden death