Familial defective apolipoprotein B-100: a mutation emerged in the mesolithic ancestors of Celtic peoples?

Atherosclerosis. 2000 Feb;148(2):433-6. doi: 10.1016/s0021-9150(99)00470-0.

Authors

A R Miserez¹, P Y Muller

Affiliation

¹ Human Molecular Genetics Groups, Research Group Genetics of Lipid Metabolism and Atherosclerosis, Departments of Research and Internal Medicine, University Clinics, Hebelstrasse 20, CH-4031, Basel, Switzerland.

PMID: 10657582
DOI: 10.1016/s0021-9150(99)00470-0

No abstract available

Publication types

Review

MeSH terms

Animals
Apolipoprotein B-100
Apolipoproteins B / genetics*
Evolution, Molecular*
Hominidae / genetics*
Humans
Hyperlipoproteinemia Type II / ethnology
Hyperlipoproteinemia Type II / genetics*
Mutation*
Switzerland / ethnology

Substances

Apolipoprotein B-100
Apolipoproteins B