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...

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Hlavní autoři:	Aleksey Nikolaevich Meshkov, Pavel Prokop'evich Malyshev, Valeriy Vladimirovich Kukharchuk, A N Meshkov, P P Malyshev, V V Kukharchuk
Médium:	Artigo
Jazyk:	Russo
Vydáno:	"Consilium Medicum" Publishing house 2009-09-01
Edice:	Терапевтический архив
Témata:	familial hypercholesterolemia ldlr and apob gene mutations coronary heart disease
On-line přístup:	https://ter-arkhiv.ru/0040-3660/article/view/30486
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