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Article

MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits.

Genes, brain, and behavior - 1 Oct 2013

Schaevitz L R, Gómez N B, Zhen D P, Berger-Sweeney J E

Abstract excerpt

Rett syndrome (RTT) is a regressive developmental disorder characterized by motor and breathing abnormalities, anxiety, cognitive dysfunction and seizures. Approximately 95% of RTT cases are caused by more than 200 different mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (Me...

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PMID: 24283265
DOI: 10.1111/gbb.12070

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24283265-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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