Author:
Wang Jun,Sun Fang,Xu Pengfei,Zhang Yufeng,Sun Xinrong,Deng Huiling
Publisher
Ovid Technologies (Wolters Kluwer Health)
Reference10 articles.
1. Clinical review on triglycerides;Laufs;Eur Heart J,2020
2. Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1;Basel-Vanagaite;Am J Hum Genet,2012
3. A compound heterozygous mutation in GPD1 causes hepatomegaly, steatohepatitis, and hypertriglyceridemia;Joshi;Eur J Hum Genet,2014
4. Expanding the molecular diversity and phenotypic spectrum of glycerol 3-phosphate dehydrogenase 1 deficiency;Dionisi-Vici;J Inherit Metab Dis,2016
5. Biallelic mutations in GPD1 gene in a Chinese boy mainly presented with obesity, insulin resistance, fatty liver, and short stature;Li;Am J Med Genet A,2017