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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Dades bibliogràfiques
Publicat a:Lipids Health Dis
Autors principals: 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
Idioma:Inglês
Publicat: BioMed Central 2016
Matèries:
Research
Accés en línia: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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