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Article

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.

Journal of medical genetics - 1 Feb 2005

Amir R E, Fang P, Yu Z, Glaze D G, Percy A K, Zoghbi H Y, Roa B B, Van den Veyver I B

Abstract excerpt

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Topics

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Share to DNA Mutational Analysis
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Share to MECP2 gene
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methyl-CpG-Binding Protein 2

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Share to Rett Syndrome

Source

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Identifiers

PMID: 15689438
DOI: 10.1136/jmg.2004.026161
PMCID: PMC1735975

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.PMID 15689438Read ↗

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