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Intermittent chylomicronemia caused by intermittent GPIHBP1 autoantibodies
Chylomicronemia caused by a deficiency in lipoprotein lipase (LPL) or GPIHBP1 (the endothelial cell protein that transports LPL to the capillary lumen) is typically diagnosed during childhood and represents a serious, lifelong medical problem. Affected patients have high plasma triglyceride levels (...
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| 出版年: | J Clin Lipidol |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7166156/ https://ncbi.nlm.nih.gov/pubmed/32107180 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacl.2020.01.012 |
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