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Article

De novo MECP2 mutation in a 46,XX male patient with Rett syndrome.

Neurogenetics - 1 Oct 2002

Maiwald Robert, Bönte Anselm, Jung Helena, Bitter Pavel, Storm Zoe, Laccone Franco, Herkenrath Peter

Abstract excerpt

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Topics

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Share to Rett Syndrome
Share to Chromosomal Proteins, Non-Histone
Share to DNA-Binding Proteins
Share to MECP2 gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Methyl-CpG-Binding Protein 2

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Share to Repressor Proteins

Source

Identifiers

PMID: 12481990
DOI: 10.1007/s10048-002-0137-5

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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De novo MECP2 mutation in a 46,XX male patient with Rett syndrome.PMID 12481990Read ↗

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Rett Syndrome: A Timely Review From Recognition to Current Clinical Approaches and Clinical Study Updates.Semantic proximity Read ↗

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Rett syndrome and the MECP2 gene.Semantic proximity Read ↗

Gene symbol: MECP2. Disease: Rett syndrome (atypical).Semantic proximity Read ↗

A rare case of a male child with post-zygotic de novo mosaic variant c.538C > T in MECP2 gene: a case report of Rett syndrome.Semantic proximity Read ↗

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