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Article

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

Brain & development - 1 Apr 2005

Li Hong, Yamagata Takanori, Mori Masato, Momoi Mariko Y

Abstract excerpt

We analyzed the FOXP2 gene, which encodes a putative transcription factor containing a polyglutamine tract and a forkhead DNA-binding domain, for a possible causative mutation in autism. FOXP2 was reported to be mutated in patients with a severe speech and language disorder. FOXP2 was located on...

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Source

Identifiers

PMID: 15737702
DOI: 10.1016/j.braindev.2004.06.002

Genes

FOXP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15737702-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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