Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia-Reference-Cited by-同舟云学术

Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia

Published:2007-11-11 Issue:12 Volume:39 Page:1483-1487
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Péterfy Miklós,Ben-Zeev Osnat,Mao Hui Z,Weissglas-Volkov Daphna,Aouizerat Bradley E,Pullinger Clive R,Frost Philip H,Kane John P,Malloy Mary J,Reue Karen,Pajukanta Päivi,Doolittle Mark H

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2007.24.pdf

Reference26 articles.

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2. Ginsberg, H.N. & Stalenhoef, A.F. The metabolic syndrome: targeting dyslipidaemia to reduce coronary risk. J. Cardiovasc. Risk 10, 121–128 (2003).

3. Pejic, R.N. & Lee, D.T. Hypertriglyceridemia. J. Am. Board Fam. Med. 19, 310–316 (2006).

4. Henderson, H.E. et al. Lipoprotein lipase activity is decreased in a large cohort of patients with coronary artery disease and is associated with changes in lipids and lipoproteins. J. Lipid Res. 40, 735–743 (1999).

5. Mead, J.R., Irvine, S.A. & Ramji, D.P. Lipoprotein lipase: structure, function, regulation, and role in disease. J. Mol. Med. 80, 753–769 (2002).

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