Reduced MeCP2 Expression is Frequent in Autism Frontal Cortex and Correlates with Aberrant MECP2 Promoter Methylation
- 23 October 2006
- journal article
- Published by Taylor & Francis in Epigenetics
- Vol. 1 (4) , 172-182
- https://doi.org/10.4161/epi.1.4.3514
Abstract
Mutations in MECP2, encoding methyl CpG binding protein 2 (MeCP2), cause most cases of Rett syndrome (RTT), an X-linked neurodevelopmental disorder. Both RTT and autism are “pervasive developmental...Keywords
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