Homozygous LPL and GPIHBP1 variants causing familial chylomicronaemia syndrome in Sri Lankan children-Reference-Cited by-同舟云学术

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Homozygous LPL and GPIHBP1 variants causing familial chylomicronaemia syndrome in Sri Lankan children

Published:2024-10 Issue:6 Volume:56 Page:904-906
ISSN:0031-3025
Container-title:Pathology
language:en
Short-container-title:Pathology

Author:

Kiyamudeen Fasilaas,Rajapaksha Madubashini,Atapattu Navoda,Kularatne Srinika D.^ORCID,Schröder Sabine,Hooper Amanda J.,Burnett John R.^ORCID,Jasinge Eresha^ORCID

Publisher

Elsevier BV

Reference13 articles.

1. Genetics of hypertriglyceridemia;Dron;Front Endocrinol (Lausanne),2020

2. A comprehensive update on the chylomicronemia syndrome;Goldberg;Front Endocrinol (Lausanne),2020

3. Lipoprotein lipase and its regulators: an unfolding story;Wu;Trends Endocrinol Metab,2021

4. Implementation of genomic medicine in Sri Lanka: initial experience and challenges;Sirisena;Appl Transl Genom,2016

5. Lipoprotein lipase deficiency in an infant with chylomicronemia, hepatomegaly, and lipemia retinalis;Vidanapathirana;Glob Pediatr Health,2017

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