Journal article icon

Journal article

Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia.

Abstract:

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 al. [2002] Brain 125:465-478) using a bilateral conjunction analysis. This searches specifically for areas of grey matter density that differ bilaterally in the affected members compared with both ...

Expand abstract
Publication status:
Published

Actions


Access Document


Publisher copy:
10.1002/hbm.10093

Authors


More by this author
Institution:
University of Oxford
Department:
Oxford, MSD, RDM, Cardiovascular Medicine
Role:
Author
Journal:
Human brain mapping
Volume:
18
Issue:
3
Pages:
194-200
Publication date:
2003-03-05
DOI:
EISSN:
1097-0193
ISSN:
1065-9471
URN:
uuid:6dcab841-e5c3-4868-96dc-7528d92854b6
Source identifiers:
28402
Local pid:
pubs:28402

Terms of use


Metrics


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP