Two common low density lipoprotein receptor gene mutations cause familial hypercholesterolemia in Afrikaners.

Familial hypercholesterolemia (FH), an autosomal dominant disease caused by mutations in the LDL receptor gene, is five times more frequent in the Afrikaner population of South Africa than it is in the population of the United States and Europe. It has been proposed that the high frequency is due to...

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Detalles Bibliográficos

Publicado en:	J Clin Invest
Autores principales:	Leitersdorf, E, Van der Westhuyzen, D R, Coetzee, G A, Hobbs, H H
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	American Society for Clinical Investigation 1989
Materias:	Research Article
Acceso en línea:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC329741/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2569482/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114258
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