Hyperlipidaemia associated with genetic variation in the apolipoprotein B gene.

Abstract:

:Common variants at the apolipoprotein B gene locus are associated with hyperlipidaemia, but conflicting data have been presented in the literature concerning the size of the effects and which polymorphisms give the best signal in the different groups of individuals studied. In this review, we will present a critique on the use and interpretation of association studies, with respect to the recent apolipoprotein B DNA polymorphism studies. The impact of these common polymorphisms and rare mutations of apolipoprotein B, primarily the substitution of arginine by glutamine at residue 3500 (R3500Q) that causes familial defective apolipoprotein B100, will also be considered.

journal_name

Curr Opin Lipidol

authors

Humphries SE,Talmud PJ

doi

10.1097/00041433-199508000-00005

subject

Has Abstract

pub_date

1995-08-01 00:00:00

pages

215-22

issue

4

eissn

0957-9672

issn

1473-6535

journal_volume

6

pub_type

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