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Article

Association of specific language impairment (SLI) to the region of 7q31.

American journal of human genetics - 1 Jun 2003

O'Brien Erin K, Zhang Xuyang, Nishimura Carla, Tomblin J Bruce, Murray Jeffrey C

Abstract excerpt

FOXP2 (forkhead box P2) was the first gene characterized in which a mutation affects human speech and language abilities. A common developmental language disorder, specific language impairment (SLI), affects 6%-7% of children with normal nonverbal intelligence and has evidence of a genetic basis in familial and twin studies. FOXP2 is located on chromosome 7q31, and studies of other disorders with speech and...

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Source

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Identifiers

PMID: 12721956
DOI: 10.1086/375403
PMCID: PMC1180313

Genes

FOXP2
CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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Semantic proximity does not establish scientific evidence.

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Association of specific language impairment (SLI) to the region of 7q31.PMID 12721956Read ↗

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Association between the FOXP2 gene and autistic disorder in Chinese population.Semantic proximity Read ↗

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