For citations:
Fetisova S.G., Yakovleva E.V., Eirich S.V., Smirnov A.A., Kostareva A.A., Zainalova Kh.Z., Pervunina T.M., Vasichkina E.S. A clinical case of a hypertrophic phenotype of cardiomyopathy in a child with a combined deficiency of oxidative phosphorylation type 3 associated with a mutation of the TSFM gene. Russian Journal for Personalized Medicine. 2024;4(3):228-237. (In Russ.) https://doi.org/10.18705/2782-3806-2024-4-4-228-237. EDN: KJGKEY