Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference30 articles.
1. Localisation of a gene implicated in a severe speech and language disorder
2. A forkhead-domain gene is mutated in a severe speech and language disorder
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5. Language fMRI abnormalities associated with FOXP2 gene mutation
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