Analysis of mutations causing familial hypercholesterolaemia in black South African patients of different ancestry

Background. Familial hypercholesterolaemia (FH) is usually caused by mutations in three genes (LDLR, APOB and PCSK9). Objective. To identify the spectrum of FH-causing mutations in black South African (SA) patients. Methods. DNA samples of 16 unrelated South African FH patients with elevated low-d...

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Bibliographic Details
Main Authors: U K Ibe, R Whittall, S E Humphries, G Pilcher, F Raal
Format: Article
Language:English
Published: South African Medical Association 2017-02-01
Series:South African Medical Journal
Subjects:
Online Access:http://www.samj.org.za/index.php/samj/article/view/11794/7949