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MECP2 gene

Known as: MECP2, METHYL-CpG-BINDING PROTEIN 2, Methyl CpG Binding Protein 2 (Rett Syndrome) Gene 
This gene plays a role in both the recognition of DNA methylation and the regulation of transcription.
National Institutes of Health

Related topics

Related topics

4 relations
DNA Methylation RegulationMethyl-CpG-Binding Protein 2Transcriptional Regulation

Narrower (1)

MECP2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Homozygous c.1160C>T (P38L) in the MECP2 gene in a female Rett syndrome patient
2010
2010
Etiopatogeneza i zasady diagnostyki molekularnej zespołu Retta
Highly Cited
2005
Highly Cited
2005
Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome
Rett syndrome (RTT; MIM 312750) is a neurodevelopmental disorder with an onset in early childhood that affects 1/10 000–1/15 000… 
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