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Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

Authors :
MacDermot, Kay D.
Bonora, Elena
Sykes, Nuala
Coupe, Anne-Marie
Lai, Cecilia S.L.
Vernes, Sonja C.
Vargha-Khadem, Faraneh
McKenzie, Fiona
Smith, Robert L.
Monaco, Anthony P.
Fisher, Simon E.
Source :
American Journal of Human Genetics. June, 2005, Vol. 76 Issue 6, p1074, 7 p.
Publication Year :
2005

Details

Language :
English
ISSN :
00029297
Volume :
76
Issue :
6
Database :
Gale General OneFile
Journal :
American Journal of Human Genetics
Publication Type :
Academic Journal
Accession number :
edsgcl.133015882