Common Genetic Variants Contribute to Primary Hypertriglyceridemia Without Differences Between Familial Combined Hyperlipidemia and Isolated Hypertriglyceridemia | Zendy

Isabel de Castro-Orós | Zendy; Ana Cenarro | Zendy; María Teresa Tejedor | Zendy; Lucía Baila-Rueda | Zendy; Rocío MateoGállego | Zendy; Itziar Lamíquiz-Moneo | Zendy; Miguel Pocovı́ | Zendy; Fernando Civeira | Zendy

Open Access

Common Genetic Variants Contribute to Primary Hypertriglyceridemia Without Differences Between Familial Combined Hyperlipidemia and Isolated Hypertriglyceridemia

Author(s) -

Isabel de Castro-Orós,

Ana Cenarro,

María Teresa Tejedor,

Lucía Baila-Rueda,

Rocío MateoGállego,

Itziar Lamíquiz-Moneo,

Miguel Pocovı́,

Fernando Civeira

Publication year - 2014

Publication title -

circulation cardiovascular genetics

Language(s) - English

Resource type - Journals

eISSN - 1942-325X

pISSN - 1942-3268

DOI - 10.1161/circgenetics.114.000522

Subject(s) - hypertriglyceridemia , genetics , biology , allele , single nucleotide polymorphism , minor allele frequency , apolipoprotein e , genotype , apolipoprotein b , hyperlipidemia , medicine , gene , endocrinology , triglyceride , cholesterol , disease , diabetes mellitus

The majority of hypertriglyceridemias are diagnosed as familial combined hyperlipidemia (FCHL) and primary isolated hypertriglyceridemias. The contribution of common genetic variants in primary hypertriglyceridemias and the genetic difference between FCHL and isolated hypertriglyceridemias have not been thoroughly examined.

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