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Article

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

European journal of human genetics : EJHG - 1 Jul 2001

Vourc'h P, Bienvenu T, Beldjord C, Chelly J, Barthélémy C, Müh J P, Andres C

Abstract excerpt

Autistic disorder is a pervasive developmental disorder considered to have a multigenic origin. Mental retardation is present in 75% of autistic patients. Autistic features are found in Rett syndrome, a neurological disorder affecting girls and associated with severe mental retardation. Recently,...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 11464249
DOI: 10.1038/sj.ejhg.5200660

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-11464249-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.PMID 11464249Read ↗

Study of MECP2 gene in Rett syndrome variants and autistic girls.Semantic proximity Read ↗

Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation.Semantic proximity Read ↗

The A140V mutation in the MECP2 gene is not a common etiological factor among Brazilian mentally retarded males.Semantic proximity Read ↗

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.Semantic proximity Read ↗

MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism.Semantic proximity Read ↗

MeCP2 gene mutation analysis in autistic boys with developmental regression.Semantic proximity Read ↗

Low significance of MECP2 mutations as a cause of mental retardation in Brazilian males.Semantic proximity Read ↗

Absence of MeCP2 mutations in patients from the South Carolina autism project.Semantic proximity Read ↗

Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation.Semantic proximity Read ↗

Identification of MeCP2 mutations in a series of females with autistic disorder.Semantic proximity Read ↗

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.Semantic proximity Read ↗

MECP2 mutations or polymorphisms in mentally retarded boys: diagnostic implications.Semantic proximity Read ↗

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