For citations:
Bukaeva A.A., Zaklyazminskaya E.V., Dombrovskaya A.V., Frolova Yu.V., Dzemeshkevich S.L. Contribution of mutations in the TNNT2 gene to the spectrum of genetic causes of DCM in Russian patients. Medical Genetics. 2020;19(5):14-15. (In Russ.) https://doi.org/10.25557/2073-7998.2020.05.14-15