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Article

Foxp2 mutations impair auditory-motor association learning.

PloS one - 1 Jan 2012

Kurt Simone, Fisher Simon E, Ehret Günter

Abstract excerpt

Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described examples of monogenic speech and language disorders. Acquisition of proficient spoken language involves auditory-guided vocal learning, a specialized form of sensory-motor association learning. The impact of etiological Foxp2 mutations on learning of auditory-motor associations in mammals has not been determined yet....

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Source

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Identifiers

PMID: 22412993
DOI: 10.1371/journal.pone.0033130
PMCID: PMC3296769

Genes

FOXP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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