Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes
Author:
Funder
Autism Speaks
Simons Foundation
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Developmental Biology,Developmental Neuroscience,Molecular Biology
Link
http://link.springer.com/content/pdf/10.1186/s13229-017-0138-8.pdf
Reference65 articles.
1. Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in x-linked mecp2, encoding methyl-cpg-binding protein 2. Nat Genet. 1999; 23(2):185–8.
2. Hagberg B, Aicardi J, Dias K, Ramos O. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett’s syndrome: report of 35 cases. Ann Neurol. 1983; 14(4):471–9.
3. Weese-Mayer DE, Lieske SP, Boothby CM, Kenny AS, Bennett HL, Silvestri JM, Ramirez JM. Autonomic nervous system dysregulation: breathing and heart rate perturbation during wakefulness in young girls with Rett syndrome. Pediatr Res. 2006; 60(4):443–9.
4. Kaufmann W, Tierney E, Rohde C, Suarez-Pedraza M, Clarke M, Salorio C, Bibat G, Bukelis I, Naram D, Lanham D, et al. Social impairments in rett syndrome: characteristics and relationship with clinical severity. J Intellect Disabil Res. 2012; 56(3):233–47.
5. Berger-Sweeney J. Cognitive deficits in Rett syndrome: what we know and what we need to know to treat them. Neurobiol Learn Mem. 2011; 96(4):637–46.
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