Familial hypercholesterolemia in Russia: genetic and phenotypic characteristics
Aim. To make qualitative and quantitative analyses of phenotypical characteristics and to study a spectrum and frequency of mutations in LDLR and APOB genes in patients with familial heterozygous hypercholesterolemia (FHHC). Material and methods. Clinical symptoms of FHHC were studied in males and f...
Main Authors: | , , , , , |
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Format: | Article |
Language: | Russian |
Published: |
"Consilium Medicum" Publishing house
2009-09-01
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Series: | Терапевтический архив |
Subjects: | |
Online Access: | https://ter-arkhiv.ru/0040-3660/article/view/30486 |