Deficits in skilled motor and auditory learning in a rat model of Rett syndrome

Abstract Background Rett syndrome is an X-linked neurodevelopmental disorder caused by a mutation in the gene MECP2. Individuals with Rett syndrome display developmental regression at an early age, and develop a range of motor, auditory, cognitive, and social impairments. Several studies have succes...

Full description

Bibliographic Details
Main Authors: Katherine S. Adcock, Abigail E. Blount, Robert A. Morrison, Amanda Alvarez-Dieppa, Michael P. Kilgard, Crystal T. Engineer, Seth A. Hays
Format: Article
Language:English
Published: BMC 2020-09-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
Online Access:http://link.springer.com/article/10.1186/s11689-020-09330-5