Erratum to: Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model

類似資料

• Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model
  著者:: Brendel, Cornelia, 等
  出版事項: (2010)
• Characterization of new-generation aminoglycoside promoting premature termination codon readthrough in cancer cells
  著者:: Bidou, Laure, 等
  出版事項: (2017)
• Characterization of the MeCP2R168X knockin mouse model for Rett syndrome.
  著者:: Eike Wegener, 等
  出版事項: (2014-01-01)
• Characterization of the MeCP2(R168X) Knockin Mouse Model for Rett Syndrome
  著者:: Wegener, Eike, 等
  出版事項: (2014)
• Design of Novel Aminoglycoside Derivatives with Enhanced Suppression of Diseases-Causing Nonsense Mutations
  著者:: Sabbavarapu, Narayana Murthy, 等
  出版事項: (2016)