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22. Apolipoprotein C-II deficiency syndrome. Clinical features, lipoprotein characterization, lipase activity, and correction of hypertriglyceridemia after apolipoprotein C-II administration in two affected patients. Baggio G; Manzato E; Gabelli C; Fellin R; Martini S; Enzi GB; Verlato F; Baiocchi MR; Sprecher DL; Kashyap ML J Clin Invest; 1986 Feb; 77(2):520-7. PubMed ID: 3944267 [TBL] [Abstract][Full Text] [Related]
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26. Apolipoprotein C-II Tuzla: a novel large deletion in APOC2 caused by Alu-Alu homologous recombination in an infant with apolipoprotein C-II deficiency. Okubo M; Toromanovic A; Ebara T; Murase T Clin Chim Acta; 2015 Jan; 438():148-53. PubMed ID: 25172036 [TBL] [Abstract][Full Text] [Related]
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28. [Familial hyperchylomicronemia with a new mutation of the lipoprotein lipase gene]. Causeret AS; Souillet AL; Marcais C; Prunetta V; Lachaux A; Faure M; Claudy A Ann Dermatol Venereol; 2001 Dec; 128(12):1343-5. PubMed ID: 11908140 [TBL] [Abstract][Full Text] [Related]
29. The familial chylomicronemia syndrome. Santamarina-Fojo S Endocrinol Metab Clin North Am; 1998 Sep; 27(3):551-67, viii. PubMed ID: 9785052 [TBL] [Abstract][Full Text] [Related]
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