Neocerebellar Crus I abnormalities associated with a speech and language disorder due to a mutation in FOXP2
Bilateral volume reduction in the caudate nucleus has been established as a prominent brain abnormality associated with a FOXP2 mutation in affected members of the ‘KE family’, who present with developmental orofacial and verbal dyspraxia in conjunction with pervasive language deficits. Despite the...
| Main Authors: | , , , , , , |
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| Format: | Journal article |
| Published: |
Springer US
2018
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