Associated Papers
The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.
Meshkov A et al.
Genes, 2021
Cholesterol Levels in Genetically Determined Familial Hypercholesterolaemia in Russian Karelia.
Korneva VA et al.
Cholesterol, 2017
Thyroglobulin gene mutations in congenital hypothyroidism.
Targovnik HM et al.
Hormone Research in Paediatrics, 2011
Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutations.
Targovnik HM et al.
Molecular and Cellular Endocrinology, 2010
[Clinical signs of homozygous familial hypercholesterolemia].
Malyshev PP et al.
Kardiologiia, 2002
[Current concepts of the pathogenesis of familial hypercholesterolemia].
Khandaker AKh et al.
Kardiologiia, 1988
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