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...
保存先:
| 出版年: | J Clin Invest |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Clinical Investigation
1989
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| 主題: | |
| オンライン･アクセス: | 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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