For citations:
Moiseeva A.M., Ivanova O.N., Emelyanchik V.S., Emelyanchik E.Yu., Marilovtseva O.V., Nikulina S.Yu., Protopopov A.V. Phenotype of heterozygous familial hypercholesterolemia caused by deletion of LDLR gene exons 2-10: a case report. Russian Journal of Cardiology. 2024;29(10S):5927. (In Russ.) https://doi.org/10.15829/1560-4071-2024-5927. EDN: LTZCMT
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