Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis-Reference-Cited by-同舟云学术

Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis

Published:2016-01 Issue:1 Volume:10 Page:92-100.e1
ISSN:1933-2874
Container-title:Journal of Clinical Lipidology
language:en
Short-container-title:Journal of Clinical Lipidology

Author:

Ariza María José,Martínez-Hernández Pedro Luis,Ibarretxe Daiana,Rabacchi Claudio,Rioja José,Grande-Aragón Cristina,Plana Nuria,Tarugi Patrizia,Olivecrona Gunilla,Calandra Sebastiano,Valdivielso Pedro

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference37 articles.

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3. Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants;Kassner;Eur J Hum Genet,2015

4. Apolipoprotein C-II Tuzla: a novel large deletion in APOC2 caused by Alu-Alu homologous recombination in an infant with apolipoprotein C-II deficiency;Okubo;Clin Chim Acta,2015

5. Two novel rare variants of APOA5 gene found in subjects with severe hypertriglyceridemia;Pisciotta;Clin Chim Acta,2011

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3. GPIHBP1 autoantibody is an independent risk factor for the recurrence of hypertriglyceridemia-induced acute pancreatitis;Journal of Clinical Lipidology;2022-09

4. A homozygous variant in the GPIHBP1 gene in a child with severe hypertriglyceridemia and a systematic literature review;Frontiers in Genetics;2022-08-16

5. Case Report: Successful Management of a 29-Day-Old Infant With Severe Hyperlipidemia From a Novel Homozygous Variant of GPIHBP1 Gene;Frontiers in Pediatrics;2022-03-10