Clinical and genetic Rett syndrome variants are defined by stable electrophysiological profiles
Rett Syndrome (RTT) is a complex neurodevelopmental disorder, frequently associated with epilepsy. Despite increasing recognition of the clinical heterogeneity of RTT and its variants (e.g Classical, Hanefeld ...
Source: BMC Pediatrics - Category: Pediatrics Authors: Conor Keogh, Giorgio Pini, Adam H. Dyer, Stefania Bigoni, Pietro DiMarco, Ilaria Gemo, Richard Reilly and Daniela Tropea Tags: Research article Source Type: research