Defects of lipoprotein metabolism in familial combined hyperlipidaemia

被引：59

作者：

de Graaf, J ^{[1
]}

Stalenhoef, AFH ^{[1
]}

机构：

[1] Univ Nijmegen Hosp, Dept Med, Div Gen Internal Med, NL-6500 HB Nijmegen, Netherlands

来源：

CURRENT OPINION IN LIPIDOLOGY | 1998年 / 9卷 / 03期

关键词：

D O I：

10.1097/00041433-199806000-00002

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Familial combined hyperlipidaemia is the most common inherited hyperlipidaemia and is found in up to 10% of patients with premature myocardial infarction, The genetic and metabolic bases of the disorder have not yet been defined. This review discusses the important advances in the past year in our understanding of the different metabolic pathways contributing to the pathogenesis of familial combined hyperlipidaemia, Curr Opin Lipidol 9;189-196. (C) 1998 Lippincott Raven Publishers.

引用

页码：189 / 196

页数：8

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