A novel APOC2 gene mutation identified in a Chinese patient with severe hypertriglyceridemia and recurrent pancreatitis

Ítems similars

• Erratum to: A novel APOC2 gene mutation identified in a Chinese patient with severe hypertriglyceridemia and recurrent pancreatitis
  per: Jiang, Jingjing, et al.
  Publicat: (2016)
• Maternal inheritance of severe hypertriglyceridemia impairs glucose metabolism in offspring
  per: Ma, Ya-Hong, et al.
  Publicat: (2015)
• AAV-Mediated ApoC2 Gene Therapy: Reversal of Severe Hypertriglyceridemia and Rescue of Neonatal Death in ApoC2-Deficient Hamsters
  per: Yang, Chun, et al.
  Publicat: (2020)
• Compound heterozygous mutations in electron transfer flavoprotein dehydrogenase identified in a young Chinese woman with late-onset glutaric aciduria type II
  per: Ying Xue, et al.
  Publicat: (2017-09-01)
• Compound heterozygous mutations in electron transfer flavoprotein dehydrogenase identified in a young Chinese woman with late-onset glutaric aciduria type II
  per: Xue, Ying, et al.
  Publicat: (2017)