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Article

Screening for mutations in the MECP2 (Rett syndrome) gene in Gilles de la Tourette syndrome.

Archives of neurology - 1 Apr 2003

Rosa Alberto L, Jankovic Joseph, Ashizawa Tetsuo

Abstract excerpt

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Topics

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Share to Chromosomal Proteins, Non-Histone
Share to DNA-Binding Proteins
Share to DNA Mutational Analysis
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methyl-CpG-Binding Protein 2

Share to Repressor Proteins

Share to Rett Syndrome

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Source

Identifiers

PMID: 12707062
DOI: 10.1001/archneur.60.4.502

Genes

MECP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screening for mutations in the MECP2 (Rett syndrome) gene in Gilles de la Tourette syndrome.PMID 12707062Read ↗

Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome.Semantic proximity Read ↗

Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases.Semantic proximity Read ↗

Evidence of somatic mosaicism for a MECP2 mutation in females with Rett syndrome: diagnostic implications.Semantic proximity Read ↗

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.Semantic proximity Read ↗

Molecular diagnosis of Rett syndrome.Semantic proximity Read ↗

Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndrome.Semantic proximity Read ↗

Rett syndrome and the MECP2 gene.Semantic proximity Read ↗

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

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.Semantic proximity Read ↗

Denaturing high-performance liquid chromatography and sequence analyses for MECP2 mutations in Rett syndrome.Semantic proximity Read ↗

Molecular Testing of MECP2 Gene in Rett Syndrome Phenotypes in Indian Girls.Semantic proximity Read ↗

Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation.Semantic proximity Read ↗

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