Two Novel Slavic Point Mutations in the Low-Density Lipoprotein Receptor Gene in Patients with Familial Hypercholesterolemia from St. Petersburg, Russia

Author:

Kh. Chakir,Skobeleva Natalia A.,Shevtsov Sergei P.,Konstantinov Vladimir O.,Denisenko Alexander D.,Schwartz Eugene I.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference10 articles.

1. Goldstein, J, L, Brown, M, S, Familial hypercholesterolemia, The Metabolic Basis of Inherited Disease, New York, McGraw-Hill, 1989, 1215, 1250

2. Association between specific apolipoprotein B polymorphism and familial defective apolipoprotein B-100;Soria;Proc Natl Acad Sci USA,1989

3. Novel deletion in the low-density lipoprotein receptor gene in a patient with familial hypercholesterolemia from Petersburg;Mandelshtam;Hum Mutation,1993

4. Low density lipoproteins of patients with ischemic heart disease. Certain physico-chemical and biological properties;Denisenko;Phys. Chem. Biol. Med.,1993

5. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia;Hobbs;Hum Mutation,1992

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