Mutations inLPL,APOC2,APOA5,GPIHBP1andLMF1in patients with severe hypertriglyceridaemia-Reference-Cited by-同舟云学术

Mutations inLPL,APOC2,APOA5,GPIHBP1andLMF1in patients with severe hypertriglyceridaemia

Published:2012-02-13 Issue:2 Volume:272 Page:185-196
ISSN:0954-6820
Container-title:Journal of Internal Medicine
language:en
Short-container-title:

Author:

Surendran R. P.,Visser M. E.,Heemelaar S.,Wang J.,Peter J.,Defesche J. C.,Kuivenhoven J. A.,Hosseini M.,Péterfy M.,Kastelein J. J. P.,Johansen C. T.,Hegele R. A.,Stroes E. S. G.,Dallinga-Thie G. M.

Publisher

Wiley

Subject

Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2796.2012.02516.x/fullpdf

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3. Monogenic pediatric dyslipidemias: classification, genetics and clinical spectrum;Rahalkar;Mol Genet Metab,2008

4. Genetic determinants of plasma triglycerides;Johansen;J Lipid Res,2011

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