Brief report: MECP2 mutations in people without Rett syndrome.

Abstract

Mutations in Methyl-CpG-Binding protein 2 (MECP2) are commonly associated with the neurodevelopmental disorder Rett syndrome (RTT). However, some people with RTT do not have mutations in MECP2, and interestingly there have been people identified with MECP2 mutations that do not have the clinical features of RTT. In this report we present four people with… (More)
DOI: 10.1007/s10803-013-1902-z

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@article{Suter2014BriefRM, title={Brief report: MECP2 mutations in people without Rett syndrome.}, author={Bernhard Suter and Diane E Treadwell-Deering and Huda Y. Zoghbi and Daniel G. Glaze and Jeffrey Lorenz Neul}, journal={Journal of autism and developmental disorders}, year={2014}, volume={44 3}, pages={703-11} }