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A novel APOC2 gene mutation identified in a Chinese patient with severe hypertriglyceridemia and recurrent pancreatitis
BACKGROUND: The severe forms of hypertriglyceridemia are usually caused by genetic defects. In this study, we described a Chinese female with severe hypertriglyceridemia caused by a novel homozygous mutation in the APOC2 gene. METHODS: Lipid profiles of the pedigree were studied in detail. LPL and H...
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| Publicado no: | Lipids Health Dis |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4715280/ https://ncbi.nlm.nih.gov/pubmed/26772541 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12944-015-0171-6 |
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