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Article

Rett syndrome and MeCP2.

Neuromolecular medicine - 1 Jun 2014

Liyanage Vichithra R B, Rastegar Mojgan

Abstract excerpt

Rett syndrome (RTT) is a severe and progressive neurological disorder, which mainly affects young females. Mutations of the methyl-CpG binding protein 2 (MECP2) gene are the most prevalent cause of classical RTT cases. MECP2 mutations or altered expression are also associated with a spectrum of neurodevelopmental disorders such as autism spectrum disorders with recent links to fetal alcohol spectrum disorders....

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Source

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Identifiers

PMID: 24615633
DOI: 10.1007/s12017-014-8295-9
PMCID: PMC5798978

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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