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Article

Language fMRI abnormalities associated with FOXP2 gene mutation.

Nature neuroscience - 1 Nov 2003

Liégeois Frédérique, Baldeweg Torsten, Connelly Alan, Gadian David G, Mishkin Mortimer, Vargha-Khadem Faraneh

Abstract excerpt

Half the members of the KE family suffer from a speech and language disorder caused by a mutation in the FOXP2 gene. We examined functional brain abnormalities associated with this mutation using two fMRI language experiments, one involving covert (silent) verb generation and the other overt (spoken) verb generation and word repetition. The unaffected family members showed a typical left-dominant distribution of...

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Source

Identifiers

PMID: 14555953
DOI: 10.1038/nn1138

Genes

FOXP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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