A novel deletion in the low-density lipoprotein receptor gene in a patient with familial hypercholesterolemia from Petersburg
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference24 articles.
1. Identification of a deletion in the LDL receptor gene A Finnish type of mutation
2. A Receptor-Mediated Pathway for Cholesterol Homeostasis
3. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
4. (1989) Familial hypercholesterolemia. In (eds): The Metabolic Basis of Inherited Disease. New York: McGraw-Hill, pp 1215-1250.
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1. Molecular diagnostics of familial hypercholesterolemia in Russia: yesterday, today and tomorrow;Medical academic journal;2024-09-11
2. Analysis of the low density lipoprotein receptor gene (<i>LDLR</i>) mutation spectrum in Russian familial hypercholesterolemia;Vavilov Journal of Genetics and Breeding;2022-06-04
3. The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia;Genes;2021-01-06
4. Familial Hypercholesterolemia in Russia: Three Decades of Genetic Studies;Frontiers in Genetics;2020-12-17
5. Familial hypercholesterolemia in St. Petersburg: Diversity of mutations argues against a strong founder effect;Russian Journal of Genetics;2007-09
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