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Article

[MECP2 gene mutations in twenty-six cases with atypical Rett syndrome].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 1 Apr 2006

Li Mei-rong, Pan Hong, Bao Xin-hua, Zhang Yu-zhi, Jiang Sheng-ling, Wu Xi-ru

Abstract excerpt

OBJECTIVE: Rett syndrome (RTT) is an X-linked progressive neurodeveopmental disorder that almost exclusively affects girls, and is one of the most common causes of mental retardation in females, with an estimated prevalence of approximately 1 in 10,000 - 15,000 female individuals. Mutations in X-linked methyl-CpG-binding protein 2 (MECP2) gene, located on chromosome Xq28, have been found to be a cause of RS. A...

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Source

Identifiers

PMID: 16780651

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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