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7. 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]
8. Recurrent acute and chronic pancreatitis in two brothers with familial chylomicronemia syndrome. Truninger K; Schmid PA; Hoffmann MM; Bertschinger P; Ammann RW Pancreas; 2006 Mar; 32(2):215-9. PubMed ID: 16552344 [TBL] [Abstract][Full Text] [Related]
9. Successful pregnancy outcome in a patient with severe chylomicronemia due to compound heterozygosity for mutant lipoprotein lipase. Al-Shali K; Wang J; Fellows F; Huff MW; Wolfe BM; Hegele RA Clin Biochem; 2002 Mar; 35(2):125-30. PubMed ID: 11983347 [TBL] [Abstract][Full Text] [Related]
10. Molecular basis of familial chylomicronemia: mutations in the lipoprotein lipase and apolipoprotein C-II genes. Reina M; Brunzell JD; Deeb SS J Lipid Res; 1992 Dec; 33(12):1823-32. PubMed ID: 1479292 [TBL] [Abstract][Full Text] [Related]
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15. Therapeutic response to medium-chain triglycerides and omega-3 fatty acids in a patient with the familial chylomicronemia syndrome. Rouis M; Dugi KA; Previato L; Patterson AP; Brunzell JD; Brewer HB; Santamarina-Fojo S Arterioscler Thromb Vasc Biol; 1997 Jul; 17(7):1400-6. PubMed ID: 9261273 [TBL] [Abstract][Full Text] [Related]
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18. A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry. Foubert L; Bruin T; De Gennes JL; Ehrenborg E; Furioli J; Kastelein J; Benlian P; Hayden M Hum Mutat; 1997; 10(3):179-85. PubMed ID: 9298816 [TBL] [Abstract][Full Text] [Related]
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