A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain

Rett syndrome (RTT) is a X-linked neurodevelopmental disorder which represents the leading cause of severe incurable intellectual disability in females worldwide. The vast majority of RTT cases are caused by mutations in the X-linked MECP2 gene, and preclinical studies on RTT largely benefit from th...

Full description

Bibliographic Details

Published in:	Neurobiology of Disease
Main Authors:	Sara Carli, Linda Chaabane, Giuseppina De Rocco, Elena Albizzati, Irene Sormonta, Stefano Calligaro, Pietro Bonizzi, Angelisa Frasca, Nicoletta Landsberger
Format:	Article
Language:	English
Published:	Elsevier 2023-05-01
Subjects:	Rett syndrome (RTT) Mecp2 mouse models In vivo MRI/MRS studies Biomarkers Neurodevelopment Neuroimaging
Online Access:	http://www.sciencedirect.com/science/article/pii/S0969996123000979