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Article

APOE epsilon4: a potential modulation factor in Rett syndrome.

Journal of child neurology - 1 May 2010

Zahorakova Daniela, Jachymova Marie, Kemlink David, Baxova Alice, Martasek Pavel

Abstract excerpt

Rett syndrome is a neurodevelopmental disorder mainly caused by de novo mutations in the MECP2 (methyl-CpG-binding protein 2) gene. There is considerable variation in the severity of clinical features among Rett syndrome patients, even among patients with the same MECP2 mutation. In addition to X...

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Source

Identifiers

PMID: 20139413
DOI: 10.1177/0883073809346848

Genes

APOE
MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20139413-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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