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References

These sources were used to develop the Genetics Home Reference condition summary on familial lipoprotein lipase deficiency.

Benlian P, De Gennes JL, Foubert L, Zhang H, Gagne SE, Hayden M. Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase gene. N Engl J Med. 1996 Sep 19;335(12):848-54. Erratum in: N Engl J Med 1997 Feb 6;336(6):451. PubMed citation
Evans V, Kastelein JJ. Lipoprotein lipase deficiency--rare or common? Cardiovasc Drugs Ther. 2002 Jul;16(4):283-7. Review. PubMed citation
Gene Review: Familial Lipoprotein Lipase Deficiency
Gilbert B, Rouis M, Griglio S, de Lumley L, Laplaud P. Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of reported mutations: 75 % are clustered in exons 5 and 6. Ann Genet. 2001 Jan-Mar;44(1):25-32. Review. PubMed citation
Mohandas MK, Jemila J, Ajith Krishnan AS, George TT. Familial chylomicronemia syndrome. Indian J Pediatr. 2005 Feb;72(2):181. PubMed citation

Reviewed: January 2008

Published: March 7, 2010