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...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2020-09-01
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Series: | Journal of Neurodevelopmental Disorders |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s11689-020-09330-5 |