Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants-Reference-Cited by-同舟云学术

Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants

Published:2015-01-14 Issue:9 Volume:23 Page:1259-1261
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Kassner Ursula,Salewsky Bastian,Wühle-Demuth Marion,Szijarto Istvan Andras,Grenkowitz Thomas,Binner Priska,März Winfried,Steinhagen-Thiessen Elisabeth,Demuth Ilja

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2014295.pdf

Reference16 articles.

1. Murad MH, Hazem A, Coto-Yglesias F et al: The association of hypertriglyceridemia with cardiovascular events and pancreatitis: a systematic review and meta-analysis. BMC Endocr Disord 2012; 12: 2.

2. Hegele RA, Ginsberg HN, Chapman MJ et al: The polygenic nature of hypertriglyceridaemia: implications for definition, diagnosis, and management. Lancet Diab Endocrinol 2014; 2: 655–666.

3. Surendran RP, Visser ME, Heemelaar S et al: Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia. J Intern Med 2012; 272: 185–196.

4. Teslovich TM, Musunuru K, Smith AV et al: Biological, clinical and population relevance of 95 loci for blood lipids. Nature 2010; 466: 707–713.

5. Wang J, Ban MR, Zou GY et al: Polygenic determinants of severe hypertriglyceridemia. Hum Mol Genet 2008; 17: 2894–2899.

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