Correction: Cas9-nickase–mediated genome editing corrects hereditary tyrosinemia in rats.

Gelijkaardige items

• Cas9-nickase–mediated genome editing corrects hereditary tyrosinemia in rats
  door: Shao, Yanjiao, et al.
  Gepubliceerd in: (2018)
• Efficient liver repopulation of transplanted hepatocyte prevents cirrhosis in a rat model of hereditary tyrosinemia type I
  door: Zhang, Ludi, et al.
  Gepubliceerd in: (2016)
• Correction to: Increasing targeting scope of adenosine base editors in mouse and rat embryos through fusion of TadA deaminase with Cas9 variants
  door: Yang, Lei, et al.
  Gepubliceerd in: (2019)
• CRISPR/Cas9-Mediated Gene Correction in Newborn Rabbits with Hereditary Tyrosinemia Type I
  door: Li, Nan, et al.
  Gepubliceerd in: (2021)
• Hereditary tyrosinemia type I. Self-induced correction of the fumarylacetoacetase defect.
  door: Kvittingen, E A, et al.
  Gepubliceerd in: (1993)