Literature DB >> 2799587

Three mutations that cause familial hypercholesterolemia in Afrikaners identified--a milestone in South African medicine.

W Gevers.   

Abstract

Entities:  

Mesh：

Year:  1989        PMID： 2799587

Source DB:  PubMed          Journal:  S Afr Med J


× No keyword cloud information.
  3 in total

1.  Familial hypercholesterolaemia.

Authors:  A David Marais
Journal:  Clin Biochem Rev       Date:  2004-02

2.  Pitfalls of relying on genetic testing only to diagnose inherited metabolic disorders in non-western populations - 5 cases of pyruvate dehydrogenase deficiency from South Africa.

Authors:  Surita Meldau; Carl Fratter; Louisa Ntombenhle Bhengu; Kate Sergeant; Kashief Khan; Gillian Tracy Riordan; Peter Allan Minham Berman
Journal:  Mol Genet Metab Rep       Date:  2020-07-22

3.  Familial hypercholesterolaemia workshop for leveraging point-of-care testing and personalised medicine in association with the Lipid and Atherosclerosis Society of Southern Africa.

Authors:  A D Marais; M J Kotze; F J Raal; A A Khine; P J Talmud; S E Humphries
Journal:  Cardiovasc J Afr       Date:  2019 Sep/Oct       Impact factor: 1.167
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.