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Small intragenic deletion of FOXP2 associated with childhood apraxia of speech and dysarthria.

Pubmed ID: 
23918746
Year: 
2013
Month: 
Sept
Volume: 
161
Issue: 
9
Citation: 
Turner S, Hildebrand MS, Block S, Damiano J, Fahey M, Reilly S, Bahlo M, Scheffer IE, Morgan AT. Small intragenic deletion of FOXP2 associated with childhood apraxia of speech and dysarthria. AMERICAN JOURNAL OF MEDICAL GENETICS PART A 161 (9) : 2321 - 2326(2013) PubMed