Subject
Gastroenterology,Hepatology,Endocrinology, Diabetes and Metabolism
Reference10 articles.
1. Familial chylomicronemia syndrome: an under-recognized cause of severe hypertriglyceridaemia;Baass;J Intern Med,2020
2. Donor splice site mutation in the apolipoprotein (Apo) C-II gene (Apo C-IIHamburg) of a patient with Apo C-II deficiency;Fojo;J Clin Investig,1988
3. Neonatal hyperlipidemia with pancreatitis: novel gene mutation of lipoprotein lipase;Shah;J Postgrad Med,2018
4. Neonatal pancreatitis associated with familial lipoprotein lipase deficiency;Siafakas;J Pediatr Gastroenterol Nutr,1999
5. Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation;Kose;J Pediatr Endocrinol Metab,2018
Cited by
1 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