Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine
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1. Research Progress on the Mechanism of Acute Hypertriglyceridemic Pancreatitis;Pancreas;2024-05-01
2. Understanding Hypertriglyceridemia: Integrating Genetic Insights;Genes;2024-01-30
3. The GPIHBP1-LPL complex and its role in plasma triglyceride metabolism: Insights into chylomicronemia;Biomedicine & Pharmacotherapy;2023-12
4. GPIHBP1 autoantibody is an independent risk factor for the recurrence of hypertriglyceridemia-induced acute pancreatitis;Journal of Clinical Lipidology;2022-09
5. A homozygous variant in the GPIHBP1 gene in a child with severe hypertriglyceridemia and a systematic literature review;Frontiers in Genetics;2022-08-16
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