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
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842266/
https://www.ncbi.nlm.nih.gov/pubmed/27108409
http://dx.doi.org/10.1186/s12944-016-0251-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842266/
https://www.ncbi.nlm.nih.gov/pubmed/27108409
http://dx.doi.org/10.1186/s12944-016-0251-2

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