Two novel mutations of the LPL gene in two Chinese family cases with familial chylomicronemia syndrome-Reference-Cited by-同舟云学术

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Two novel mutations of the LPL gene in two Chinese family cases with familial chylomicronemia syndrome

Published:2021-10 Issue: Volume:521 Page:264-271
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Wang Mingying,Zhou Yuantao,He Xiaoli,Deng Chengjun,Liu Xiaoning,Li Juan,Zhou Lin,Li Ying,Zhang Yu,Liu Haifeng,Li Li

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference32 articles.

1. Cholesteryl ester transfer protein inhibitors: challenges and perspectives;Filippatos;Expert Rev Cardiovasc Ther.,2016

2. Practical definitions of severe versus familial hypercholesterolaemia and hypertriglyceridaemia for adult clinical practice;Garg;Lancet Diabetes Endocrinol.,2019

3. High frequency of lipoprotein lipase deficiency in the Quebec population;Julien;Can J Cardiol.,1992

4. Diagnostic algorithm for familial chylomicronemia syndrome;Stroes;Atheroscler Suppl.,2017

5. Low seroprevalance of diphtheria, tetanus and pertussis in ambulatory adult patients: the need for lifelong vaccination;Tanriover;Eur J Intern Med.,2014

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The GPIHBP1-LPL complex and its role in plasma triglyceride metabolism: Insights into chylomicronemia;Biomedicine & Pharmacotherapy;2023-12

2. Familial chylomicronemia syndrome caused by compound heterozygous mutation of lipoprotein lipase gene: A case report and review of literature;Clinica Chimica Acta;2022-12

3. Efficacy and safety of the apolipoprotein C-III inhibitor Volanesorsen: a systematic evaluation and meta-analysis;Endocrine;2022-03-17

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