The Role of MeCP2 in Brain Development and Neurodevelopmental Disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health
Link
http://www.springerlink.com/index/pdf/10.1007/s11920-010-0097-7
Reference51 articles.
1. Hammer S, Dorrani N, Dragich J, et al.: The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome. Ment Retard Dev Disabil Res Rev 2002, 8:94–98.
2. Zoghbi HY: MeCP2 dysfunction in humans and mice. J Child Neurol 2005, 20:736–740.
3. Girard M, Couvert P, Carrie A, et al.: Parental origin of de novo MECP2 mutations in Rett syndrome. Eur J Hum Genet 2001, 9:231–236.
4. Trappe R, Laccone F, Cobilanschi J, et al.: MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin. Am J Hum Genet 2001, 68:1093–1101.
5. Amir RE, Van den Veyver IB, Wan M, et al.: Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl- CpG-binding protein 2. Nat Genet 1999, 23:185–188.
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