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Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

✍ Scribed by Kay D. MacDermot; Elena Bonora; Nuala Sykes; Anne-Marie Coupe; Cecilia S.L. Lai; Sonja C. Vernes; Faraneh Vargha-Khadem; Fiona McKenzie; Robert L. Smith; Anthony P. Monaco; Simon E. Fisher

Book ID: 117854632
Publisher: American Society of Human Genetics
Year: 2005
Tongue: English
Weight: 205 KB
Volume: 76
Category: Article
ISSN: 0002-9297
DOI: 10.1086/430841

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