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Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia
The KE family is a large three‐generational pedigree in which half of the members suffer from a verbal and orofacial dyspraxia in association with a point mutation in the FOXP2 gene. This report extends previous voxel‐based morphometric analyses of magnetic resonance imaging (MRI) scans (Watkins et...
Salvato in:
| Pubblicato in: | Hum Brain Mapp |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wiley Subscription Services, Inc., A Wiley Company
2003
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6872113/ https://ncbi.nlm.nih.gov/pubmed/12599277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hbm.10093 |
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