Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia

OBJECTIVE: The severe forms of hypertriglyceridaemia (HTG) are caused by mutations in genes that lead to loss of function of lipoprotein lipase (LPL). In most patients with severe HTG (TG >10 mmol/L) it is a challenge to define the underlying cause. We investigated the molecular basis of severe H...

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Detalhes bibliográficos
Main Authors: Surendran, R Preethi, Visser, Maartje E, Heemelaar, Steffie, Wang, Jian, Peter, Jorge, Defesche, Joep C, Kuivenhoven, Jan A, Hosseini, Maryam, Péterfy, Miklós, Kastelein, John JP, Johansen, Chris T, Hegele, Robert A, Stroes, Erik SG, Dallinga-Thie, Geesje M
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3940136/
https://ncbi.nlm.nih.gov/pubmed/22239554
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2796.2012.02516.x
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