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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發表在: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
格式: Artigo
語言:Inglês
出版: BioMed Central 2016
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Research
在線閱讀: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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