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. 2010 Mar 24;12(2):127–134. doi: 10.1007/s11920-010-0097-7

Fig. 1.

Fig. 1

Association of neurodevelopmental disorders with specific classes of Methyl CpG binding protein-2 (MeCP2) mutation. The schematic diagram depicts the major MeCP2-based neurodevelopmental disorders and their association with each class of MeCP2 mutation. RTT—Rett syndrome; XLMR—X-linked mental retardation