L Hinz, J Torrella Barrufet, VM Heine - Acta neuropathologica …, 2019 - Springer
Rett Syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the Methyl
CpG binding protein 2 (MECP2) gene. Deficient K+-Cl—co-transporter 2 (KCC2) expression …