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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Detalles Bibliográficos
Publicado en: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
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2016
Assuntos:
Research
Acceso en liña: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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