Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry-Reference-Cited by-同舟云学术

Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry

Published:1999-05 Issue:5 Volume:55 Page:340-345
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Loubser Odell,Marais A David,Kotze Maritha J,Godenir Nicole,Thiart Rochelle,Scholtz Charlotte L,De Villiers J Nico P,Hillermann Renate,Firth Jean C,Weich Hellmuth Fh,Maritz Frans,Jones Sheena,Van Der Westhuyzen Deneys R

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.1999.550507.x/fullpdf

Reference36 articles.

1. Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100;Soria;Proc Natl Acad Sci,1989

2. A host of hypercholesterolaemic homozygotes in South Africa;Seftel;Br Med J,1980

3. Prevalence of familial hypercholesterolemia in Johannesburg Jews;Seftel;Am J Med Genet,1989

4. Familial defective apolipoprotein-B is rare in hypercholesterolaemic South African Afrikaners, Coloureds and Indians;Rubinsztein;S Afr Med J,1995

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