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FOXP2 wt Allele

Known as: SPCH1, DKFZp686H1726, CAGH44 
Human FOXP2 wild-type allele is located in the vicinity of 7q31 and is approximately 279 kb in length. This allele, which encodes forkhead box… 
National Institutes of Health

Related topics

Related topics

8 relations
Apraxia, Developmental VerbalChromosome 7q31FOXP2 geneHomo sapiens

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
Trastorno específico del desarrollo del lenguaje: una aproximación teórica a su diagnóstico, etiología y manifestaciones clínicas
Objetivo. Se presenta una revision teorica actualizada de la definicion, los criterios diagnosticos, las propuestas de… 
Review
2004
Review
2004
[Specific developmental language disorder: a theoretical approach to its diagnosis, aetiology and clinical symptoms].
AIM This article presents an updated review about the definition, diagnostic criteria, classifications, etiology and the… 
Highly Cited
2002
Highly Cited
2002
FOXP2: novel exons, splice variants, and CAG repeat length stability
Abstract. FOXP2 is a transcription factor containing a polyglutamine tract, a zinc-finger motif, and a forkhead DNA-binding… 
Highly Cited
2002
Highly Cited
2002
FOXP 2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment
The FOXP2 gene, located on human 7q31 (at the SPCH1 locus), encodes a transcription factor containing a polyglutamine tract and a… 
2002
2002
Towards the elucidation of the genetic and brain bases of developmental speech and language disorders.
Two papers in this issue of Brain by Watkins and colleagues (Watkins et al ., 2002 a , b ) provide fascinating and important new… 
2001
2001
First Gene Linked to Speech Identified
Only human beings can string a complex series of sounds together into speech. Now a team of researchers has identified the first… 
Highly Cited
1997
Highly Cited
1997
Localisation of a gene implicated in a severe speech and language disorder
Between 2 and 5% of children who are otherwise unimpaired have significant difficulties in acquiring expressive and/or receptive… 
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