Language fMRI abnormalities associated with FOXP2 gene mutation
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Neuroscience
Link
http://www.nature.com/articles/nn1138.pdf
Reference34 articles.
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2. Fisher, S.E., Vargha-Khadem, F., Watkins, K.E., Monaco, A.P. & Pembrey, M.E. Localisation of a gene implicated in severe speech and language disorder. Nat. Genet. 18, 168–170 (1998).
3. Vargha-Khadem, F., Watkins, K.E., Alcock, K.J., Fletcher, P. & Passingham, R.E. Praxic and non-verbal cognitive deficits in a large family with a genetically transmitted speech and language disorder. Proc. Natl. Acad. Sci. USA 92, 930–933 (1995).
4. Alcock, K.J., Passingham, R.E., Watkins, K.E. & Vargha-Khadem, F. Oral dyspraxia in inherited speech and language impairment and acquired dysphasia. Brain Lang. 75, 17–33 (2000).
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