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
Article in Russian Journal for Personalized Medicine (August 2024)
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Article in Russian Journal for Personalized Medicine (August 2024)
Article in Molecular Biology Reports (April 2024)
Article in Cells (August 2022)