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2. Novel LPL mutations associated with lipoprotein lipase deficiency: two case reports and a literature review. Rahalkar AR; Giffen F; Har B; Ho J; Morrison KM; Hill J; Wang J; Hegele RA; Joy T Can J Physiol Pharmacol; 2009 Mar; 87(3):151-60. PubMed ID: 19295657 [TBL] [Abstract][Full Text] [Related]
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6. A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians. Ma Y; Henderson HE; Murthy V; Roederer G; Monsalve MV; Clarke LA; Normand T; Julien P; Gagné C; Lambert M N Engl J Med; 1991 Jun; 324(25):1761-6. PubMed ID: 2038366 [TBL] [Abstract][Full Text] [Related]
7. A mutation in the lipoprotein lipase gene is the molecular basis of chylomicronemia in a colony of domestic cats. Ginzinger DG; Lewis ME; Ma Y; Jones BR; Liu G; Jones SD J Clin Invest; 1996 Mar; 97(5):1257-66. PubMed ID: 8636438 [TBL] [Abstract][Full Text] [Related]
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10. A compound heterozygote for a novel missense mutation (G105R) in exon 3 and a missense mutation (D204E) in exon 5 of the lipoprotein lipase gene in a Japanese infant with hyperchylomicronaemia. Ikeda Y; Goji K; Takagi A Clin Sci (Lond); 2000 Dec; 99(6):569-78. PubMed ID: 11099402 [TBL] [Abstract][Full Text] [Related]
11. [A gene analysis of familial lipoprotein lipase deficiency in China]. Shen J; Chen R; Hu W; Bingshen KE; Li L; Du Y; Liu Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Aug; 16(4):233-5. PubMed ID: 10431049 [TBL] [Abstract][Full Text] [Related]
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20. 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] [Next] [New Search]