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Article

FOXP2 is not a major susceptibility gene for autism or specific language impairment.

American journal of human genetics - 1 May 2002

Newbury D F, Bonora E, Lamb J A, Fisher S E, Lai C S L, Baird G, Jannoun L, Slonims V, Stott C M, Merricks M J, Bolton P F, Bailey A J, Monaco A P

Abstract excerpt

The FOXP2 gene, located on human 7q31 (at the SPCH1 locus), encodes a transcription factor containing a polyglutamine tract and a forkhead domain. FOXP2 is mutated in a severe monogenic form of speech and language impairment, segregating within a single large pedigree, and is also disrupted by a translocation in an isolated case. Several studies of autistic disorder have demonstrated linkage to a similar region...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 11894222
DOI: 10.1086/339931
PMCID: PMC447606

Genes

FOXP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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FOXP2 is not a major susceptibility gene for autism or specific language impairment.PMID 11894222Read ↗

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Evaluation of FOXP2 as an autism susceptibility gene.Semantic proximity Read ↗

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Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.Semantic proximity Read ↗

Mutation screening of FOXP2 in individuals diagnosed with autistic disorder.Semantic proximity Read ↗

Association of specific language impairment (SLI) to the region of 7q31.Semantic proximity Read ↗

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.Semantic proximity Read ↗

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