Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Anne-Marie Coupe"'
Autor:
Julie A. Coventry, Jérôme Nicod, Simon E. Fisher, Niamh Kenny, Fanny M. Elahi, Anne-Marie Coupe, Louise E. Bird, Kay E. Davies, Sonja C. Vernes
Publikováno v:
Human Molecular Genetics
Mutations in the FOXP2 gene cause a severe communication disorder involving speech deficits (developmental verbal dyspraxia), accompanied by wide-ranging impairments in expressive and receptive language. The protein encoded by FOXP2 belongs to a dive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::107d3b5369c2394a9e67f0c0ffc3ce23
https://doi.org/10.1093/hmg/ddl392
https://doi.org/10.1093/hmg/ddl392
Autor:
Simon E. Fisher, Anne-Marie Coupe, Christopher Preece, Klaus Rajewsky, Catherine A. French, Matthias Groszer
Publikováno v:
Genesis
Genesis (New York, N.y. : 2000)
Genesis (New York, N.y. : 2000)
Disruptions of the human FOXP2 gene cause problems with articulation of complex speech sounds, accompanied by impairment in many aspects of language ability. The FOXP2/Foxp2 transcription factor is highly similar in humans and mice, and shows a compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74dff7cff25f1bd615c4db21387825a0
https://hdl.handle.net/11858/00-001M-0000-0012-CB13-011858/00-001M-0000-0012-CB14-E
https://hdl.handle.net/11858/00-001M-0000-0012-CB13-011858/00-001M-0000-0012-CB14-E
Autor:
Robert L. Smith, Elena Bonora, Fiona Haslam McKenzie, Kay D. MacDermot, Anne Marie Coupe, Sonja C. Vernes, Simon E. Fisher, Nuala Sykes, Cecilia S. L. Lai, Faraneh Vargha-Khadem, Anthony P. Monaco
Publikováno v:
American Journal of Human Genetics
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a unique entry point into neuromolecular mechanisms influencing human speech and language acquisition. In multiple members of the well-studied KE family,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55b695581810c391830031321112e865
https://pubmed.ncbi.nlm.nih.gov/15877281
https://pubmed.ncbi.nlm.nih.gov/15877281
