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Article

Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways.

Genomics - 1 Jan 2011

Colak Dilek, Al-Dhalaan Hesham, Nester Michael, Albakheet Albandary, Al-Younes Banan, Al-Hassnan Zohair, Al-Dosari Mohammad, Chedrawi Aziza, Al-Owain Muhammad, Abudheim Nada, Al-Alwan Laila, Al-Odaib Ali, Ozand Pinar, Inan Mehmet Sait, Kaya Namik

Abstract excerpt

Rett syndrome (RTT) is an X-linked neurodevelopmental disorder characterized by derangements in nervous system especially in cognition and behavior. The present study aims to understand the molecular underpinnings of two subtypes of RTT, classic RTT and Rett-like, and to elucidate common pathways...

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Identifiers

PMID: 20934504
DOI: 10.1016/j.ygeno.2010.09.004

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20934504-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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