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    • Glial Dysfunction in MeCP2 Deficiency Models: Implications for Rett Syndrome 

      Kahanovitch, Uri; Patterson, Kelsey C.; Hernandez, Raymundo; Olsen, Michelle L. (MDPI, 2019-08-05)
      Rett syndrome (RTT) is a rare, X-linked neurodevelopmental disorder typically affecting females, resulting in a range of symptoms including autistic features, intellectual impairment, motor deterioration, and autonomic ...