Anxiety-like behavior in Rett syndrome: characteristics and assessment by anxiety scales-Reference-Cited by-同舟云学术

Anxiety-like behavior in Rett syndrome: characteristics and assessment by anxiety scales

Published:2015-09-15 Issue:1 Volume:7 Page:
ISSN:1866-1947
Container-title:Journal of Neurodevelopmental Disorders
language:en
Short-container-title:J Neurodevelop Disord

Author:

Barnes Katherine V.,Coughlin Francesca R.,O’Leary Heather M.,Bruck Natalie,Bazin Grace A.,Beinecke Emily B.,Walco Alexandra C.,Cantwell Nicole G.,Kaufmann Walter E.

Publisher

Springer Science and Business Media LLC

Subject

Cognitive Neuroscience,Clinical Neurology,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1186/s11689-015-9127-4

Reference59 articles.

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2. 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.

3. Cuddapah VA, Pillai RB, Shekar KV, Lane JB, Motil KJ, Skinner SA, et al. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. J Med Genet. 2014;51(3):152–8.

4. Neul JL, Lane JB, Lee HS, Geerts S, Barrish JO, Annese F, et al. Developmental delay in Rett syndrome: data from the natural history study. J Neurodev Disord. 2014;6(1):20.

5. Kaufmann WE, Johnston MV, Blue ME. MeCP2 expression and function during brain development: implications for Rett syndrome’s pathogenesis and clinical evolution. Brain Dev. 2005;27 Suppl 1:S77–87.

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