Identification of three mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians-Reference-Cited by-同舟云学术

Identification of three mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians

Published:1998 Issue:S1 Volume:11 Page:S226-S231
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Couture Patrick,Vohl Marie-Claude,Gagné Claude,Gaudet Daniel,Torres Ana L.,Lupien Paul J.,Després Jean-Pierre,Labrie Fernand,Simard Jacques,Moorjani Sital

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference12 articles.

1. Disulfide bridges of a cysteine -rich repeat of the LDL receptor ligand-binding domain;Bieri;Biochemistry,1995

2. The CpG dinucleotide and human genetic disease;Cooper;Hum Genet,1988

3. Detection of the apoB-3500 mutation (glutamine for arginine) by gene amplification and cleavage with MspI;Hansen;J Lipid Res,1991

4. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia;Hobbs;Hum Mutat,1992

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