Frequency of rare mutations and common genetic variations in severe hypertriglyceridemia in the general population of Spain

BACKGROUND: Hypertriglyceridemia (HTG) is a common complex metabolic trait that results of the accumulation of relatively common genetic variants in combination with other modifier genes and environmental factors resulting in increased plasma triglyceride (TG) levels. The majority of severe primary...

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Bibliografiske detaljer
Udgivet i:Lipids Health Dis
Main Authors: Lamiquiz-Moneo, Itziar, Blanco-Torrecilla, Cristian, Bea, Ana M., Mateo-Gallego, Rocío, Pérez-Calahorra, Sofía, Baila-Rueda, Lucía, Cenarro, Ana, Civeira, Fernando, de Castro-Orós, Isabel
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2016
Fag:
Research
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4842266/
https://ncbi.nlm.nih.gov/pubmed/27108409
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12944-016-0251-2
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