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    • Studying synaptopathies using Mecp2 transgenic mouse models 

      Bodda, Chiranjeevi (2013-09-05)
      The MECP2 gene is located in the Xq28, which encodes for methyl-CpG binding protein 2 (MeCP2). Mutations in MECP2 gene is the primary cause of postnatal neurodevelopmental disorder, Rett syndrome (RTT) (loss-of-function). ...