Tangier disease: a structural defect in apolipoprotein A-I (apoA-I Tangier).
Tangier disease is a familial disorder characterized by orange tonsils, cholesterol ester deposition in reticuloendothelial cells, abnormal chylomicron remnants, and a marked reduction in high density lipoproteins. Plasma concentrations of the apolipoproteins apo-A-I and apoA-II in patients with Tan...
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| Опубликовано в:: | Proc Natl Acad Sci U S A |
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| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
National Academy of Sciences
1982
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC346223/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6806810/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.79.8.2485 |
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