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3. Molecular and functional characterization of familial chylomicronemia syndrome. Teramoto R; Tada H; Kawashiri MA; Nohara A; Nakahashi T; Konno T; Inazu A; Mabuchi H; Yamagishi M; Hayashi K Atherosclerosis; 2018 Feb; 269():272-278. PubMed ID: 29153744 [TBL] [Abstract][Full Text] [Related]
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6. Acute pancreatitis risk in multifactorial chylomicronemia syndrome depends on the molecular cause of severe hypertriglyceridemia. Guay SP; Paquette M; Taschereau A; Girard L; Desgagné V; Bouchard L; Bernard S; Baass A Atherosclerosis; 2024 May; 392():117489. PubMed ID: 38448342 [TBL] [Abstract][Full Text] [Related]
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10. 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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12. The molecular basis of familial chylomicronemia. Ameis D; Schotz C; Greten H Z Gastroenterol Verh; 1991 Mar; 26():102-3. PubMed ID: 1714114 [No Abstract] [Full Text] [Related]
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17. Pancreatitis polygenic risk score is associated with acute pancreatitis in multifactorial chylomicronemia syndrome. Guay SP; Paquette M; Taschereau A; Desgagné V; Bouchard L; Bernard S; Baass A J Clin Lipidol; 2024; 18(3):e413-e422. PubMed ID: 38443284 [TBL] [Abstract][Full Text] [Related]