The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia

Prevalence of Familial Hypercholesterolemia Among the General Population and Patients With Atherosclerotic Cardiovascular Disease

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Worldwide Prevalence of Familial Hypercholesterolemia

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Analysis Of The Ldlr, Apob, Pcsk9 And Ldlrap1 Genes Variability In Patients With Familial Hypercholesterolemia In West Siberia Using Targeted High Throughput Resequencing

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The complex molecular genetics of familial hypercholesterolaemia

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ClinVar database of global familial hypercholesterolemia-associated DNA variants

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Analysis of publicly available LDLR, APOB, and PCSK9 variants associated with familial hypercholesterolemia: application of ACMG guidelines and implications for familial hypercholesterolemia diagnosis

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The Mobile Element Locator Tool (MELT): population-scale mobile element discovery and biology

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The UCL low-density lipoprotein receptor gene variant database: pathogenicity update

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Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society

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Familial hypercholesterolemia mutations in Petrozavodsk: no similarity to St. Petersburg mutation spectrum

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“Finnish” Mutations in LDL Receptor Gene: A Rare Cause of Familial Hypercholesterolemia in St. Petersburg and Petrozavodsk

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New mutations in low-density lipoprotein receptor gene in familial hypercholesterolemia patients from Petrozavodsk

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Integrative genomics viewer

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The spectrum of mutations in the low-density lipoprotein receptor gene in the Russian population

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