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Article

FOXP2: novel exons, splice variants, and CAG repeat length stability.

Human genetics - 1 Aug 2002

Bruce Heather A, Margolis Russell L

Abstract excerpt

FOXP2 is a transcription factor containing a polyglutamine tract, a zinc-finger motif, and a forkhead DNA-binding domain. The FOXP2 gene is located on 7q31. A missense mutation in the forkhead domain (exon 14) and a balanced reciprocal translocation t(5;7)(q22;q31.2) with a breakpoint between exo...

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Source

Identifiers

PMID: 12189486
DOI: 10.1007/s00439-002-0768-5

Genes

FOXP2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-12189486-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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