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...

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Dades bibliogràfiques
Publicat a:Hum Brain Mapp
Autors principals: Belton, Emma, Salmond, Claire H., Watkins, Kate E., Vargha‐Khadem, Faraneh, Gadian, David G.
Format: Artigo
Idioma:Inglês
Publicat: Wiley Subscription Services, Inc., A Wiley Company 2003
Matèries:
Research Articles
Accés en línia: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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