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

Samankaltaisia teoksia

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