CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR

CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR

Clinical case of a patient with family hypercholesterolemia caused by mutation c.1859G>C (p.W620S) in the gene of human low density lipoproteins receptor.

Bibliographic Details
Main Authors:	V. A. Korneva, T. Yu. Kuznetsova, T. Yu. Bogoslovskaya, R. Z. Murtazina, A. V. Didio, M. P. Serebrenitskaya, V. O. Konstantinov, M. Yu. Mandelshtam, V. B. Vasiliev
Format:	Article
Language:	Russian
Published:	«SILICEA-POLIGRAF» LLC 2015-12-01
Series:	Кардиоваскулярная терапия и профилактика
Online Access:	https://cardiovascular.elpub.ru/jour/article/view/282

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