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Article

[FOXP2 and the molecular biology of language: new evidence. I. Phenotypic aspects and animal models].

Revista de neurologia - 1 Jan 2000

Benítez-Burraco A

Abstract excerpt

INTRODUCTION: FOXP2 is the first gene linked to a hereditary variant of specific language impairment and seems to code for a transcriptional repressor that intervenes in the regulation of development and the functioning of certain thalamic-cortical-striatal circuits. DEVELOPMENT: In the last three years significant progress has been made in the analysis of the structural and functional properties of the gene. The...

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Identifiers

PMID: 18351569

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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