Open AccessCLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR
Author(s) -
В. А. Корнева,
Т. Ю. Кузнецова,
Т. Ю. Богословская,
Anna Didio,
М. П. Серебреницкая,
В. О. Константинов,
М. Ю. Мандельштам,
В. Б. Васильев
Publication year - 2015
Publication title -
kardiovaskulârnaâ terapiâ i profilaktika
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.158
H-Index - 16
eISSN - 2619-0125
pISSN - 1728-8800
DOI - 10.15829/1728-8800-2015-6-52-53
Subject(s) - medicine , familial hypercholesterolemia , mutation , ldl receptor , gene , endocrinology , genetics , cholesterol , lipoprotein , biology