These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
15. Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome. Lam CW; Yuen YP; Cheng WF; Chan YW; Tong SF Clin Chim Acta; 2006 Feb; 364(1-2):256-9. PubMed ID: 16153625 [TBL] [Abstract][Full Text] [Related]
16. A Novel APOC2 Missense Mutation Causing Apolipoprotein C-II Deficiency With Severe Triglyceridemia and Pancreatitis. Ueda M; Dunbar RL; Wolska A; Sikora TU; Escobar MDR; Seliktar N; deGoma E; DerOhannessian S; Morrell L; McIntyre AD; Burke F; Sviridov D; Amar M; Shamburek RD; Freeman L; Hegele RA; Remaley AT; Rader DJ J Clin Endocrinol Metab; 2017 May; 102(5):1454-1457. PubMed ID: 28201738 [TBL] [Abstract][Full Text] [Related]
17. Enhanced susceptibility to pancreatitis in severe hypertriglyceridaemic lipoprotein lipase-deficient mice and agonist-like function of pancreatic lipase in pancreatic cells. Wang Y; Sternfeld L; Yang F; Rodriguez JA; Ross C; Hayden MR; Carriere F; Liu G; Hofer W; Schulz I Gut; 2009 Mar; 58(3):422-30. PubMed ID: 18936103 [TBL] [Abstract][Full Text] [Related]
18. Familial chylomicronemia syndrome- an uncommon cause of acute pancreatitis with encephalopathy. Kota SK; Kota SK; Jammula S; Modi KD Indian J Gastroenterol; 2012 Sep; 31(5):277-9. PubMed ID: 23081844 [No Abstract] [Full Text] [Related]
19. A novel substitution at the translation initiator codon (ATG-->ATC) of the lipoprotein lipase gene is mainly responsible for lipoprotein lipase deficiency in a patient with severe hypertriglyceridemia and recurrent pancreatitis. Yu XH; Zhao TQ; Wang L; Liu ZP; Zhang CM; Chen R; Li L; Liu G; Hu WC Biochem Biophys Res Commun; 2006 Mar; 341(1):82-7. PubMed ID: 16431216 [TBL] [Abstract][Full Text] [Related]