Functionality of sequence variants in the genes coding for the low-density lipoprotein receptor and apolipoprotein B in individuals with inherited hypercholesterolemia-Reference-Cited by-同舟云学术

Functionality of sequence variants in the genes coding for the low-density lipoprotein receptor and apolipoprotein B in individuals with inherited hypercholesterolemia

Published:2010-04-13 Issue:6 Volume:31 Page:752-760
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Huijgen Roeland,Kindt Iris,Fouchier Sigrid W.,Defesche Joep C.,Hutten Barbara A.,Kastelein John J.P.,Vissers Maud N.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference27 articles.

1. The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier gene;Abifadel;Hum Mutat,2009

2. Outcome of case finding among relatives of patients with known heterozygous familial hypercholesterolaemia;Bhatnagar;BMJ,2000

3. The molecular mechanism for the genetic disorder familial defective apolipoprotein B100;Boren;J Biol Chem,2001

4. Defesche JC Kastelein JJ www.jojogenetics.nl 2010

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