Identification of the apo B-3500 mutation in the Norwegian population

Familial defective apolipoprotein B-100 (FDB) is caused by a mutation in codon 3500 of the apo B gene. It is inherited in a co-dominant fashion and is characterized by hypercholesterolaemia Thus, FDB has similar features to familial hypercholesterolaemia (FH). In order to investigate whether some of...

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Veröffentlicht in:	Scandinavian journal of clinical and laboratory investigation 1995, Vol.55 (3), p.217-221
Hauptverfasser:	Leren, T. P., Rosdningen, O. K., Tonstad, S., Rossby, O., Urdal, P., Ose, L.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult apolipoprotein B Apolipoproteins B - genetics Biological and medical sciences Child Cholesterol - blood DNA - analysis Female Fundamental and applied biological sciences. Psychology General aspects Genes, Dominant Haplotypes - genetics Heterozygote Humans hypercholesterolemia Hyperlipoproteinemia Type II - ethnology Hyperlipoproteinemia Type II - genetics Male mutation Norway Point Mutation Receptors, LDL - genetics Vertebrates: cardiovascular system
Online-Zugang:	Volltext
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