The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
About this item
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Author / Creator
Publisher
Berlin/Heidelberg: Springer-Verlag
Journal title
Language
English
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Publisher
Berlin/Heidelberg: Springer-Verlag
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Scope and Contents
Contents
Rare disruptions of
FOXP2
have been strongly implicated in deficits in language development. Research over the past decade has suggested a role in the formation of underlying neural circuits required for speech. Until recently no evidence existed to suggest that the closely related
FOXP1
gene played a role in neurodevelopmental processe...
Alternative Titles
Full title
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
Authors, Artists and Contributors
Author / Creator
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3470686
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3470686
Other Identifiers
ISSN
0340-6717
E-ISSN
1432-1203
DOI
10.1007/s00439-012-1193-z
