Author:
Bruin T.,Tuzgöl S.,Mulder W.J.,van den Ende A.E.,Jansen H.,Hayden M.R.,Kastelein J.J.
Subject
Cell Biology,Endocrinology,Biochemistry
Cited by
13 articles.
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1. Mutations inLPL,APOC2,APOA5,GPIHBP1andLMF1in patients with severe hypertriglyceridaemia;Journal of Internal Medicine;2012-02-13
2. The relative importance of common and rare genetic variants in the development of hypertriglyceridemia;Expert Review of Cardiovascular Therapy;2011-05
3. Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia;Atherosclerosis;2011-02
4. Association Analyses of Genetic Polymorphisms of GSTM1, GSTT1, NQO1, NAT2, LPL, PRSS1, PSTI, and CFTR With Chronic Alcoholic Pancreatitis in Japan;Alcoholism: Clinical and Experimental Research;2010-02
5. Compound heterozygosity of novel missense mutations (Ser45→Gly, Cys278→Arg) in the lipoprotein lipase gene in a newborn Korean infant;Clinica Chimica Acta;2008-01