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Social impairments in Rett syndrome: characteristics and relationship with clinical severity

✍ Scribed by W. E. Kaufmann; E. Tierney; C. A. Rohde; M. C. Suarez-Pedraza; M. A. Clarke; C. F. Salorio; G. Bibat; I. Bukelis; D. Naram; D. C. Lanham; S. Naidu

Book ID: 114741457
Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 146 KB
Volume: 56
Category: Article
ISSN: 0964-2633
DOI: 10.1111/j.1365-2788.2011.01404.x

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## Abstract Rett syndrome (RTT; OMIM 312750) is an X‐linked dominant neurodevelopmental disorder leading to cognitive and motor impairment, epilepsy, and autonomic dysfunction in females. Since the discovery that RTT is caused by mutations in __MECP2__, large retrospective genotype–phenotype correl