Defects of lipoprotein metabolism in familial combined hyperlipidaemia.

Abstract:

: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.

journal_name

Curr Opin Lipidol

authors

de Graaf J,Stalenhoef AF

doi

10.1097/00041433-199806000-00002

subject

Has Abstract

pub_date

1998-06-01 00:00:00

pages

189-96

issue

3

eissn

0957-9672

issn

1473-6535

journal_volume

9

pub_type

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