Journal article icon

Journal article

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.

Abstract:

Neurodevelopmental disorders that disturb speech and language are highly heritable. Isolation of the underlying genetic risk factors has been hampered by complexity of the phenotype and potentially large number of contributing genes. One exception is the identification of rare heterozygous mutations of the FOXP2 gene in a monogenic syndrome characterised by impaired sequencing of articulatory gestures, disrupting speech (developmental verbal dyspraxia, DVD), as well as multiple deficits in ex...

Expand abstract
Publication status:
Published

Actions


Access Document


Publisher copy:
10.1038/ejhg.2009.43

Authors


Vernes, SC More by this author
MacDermot, KD More by this author
More by this author
Institution:
University of Oxford
Department:
Oxford, MSD, Clinical Medicine, WTC Human Genetics
More by this author
Institution:
University of Oxford
Department:
Oxford, MSD, Clinical Medicine, WTC Human Genetics
Journal:
European journal of human genetics : EJHG
Volume:
17
Issue:
10
Pages:
1354-1358
Publication date:
2009-10-05
DOI:
EISSN:
1476-5438
ISSN:
1018-4813
URN:
uuid:25b9edd7-76a6-4163-a11f-ec544b312973
Source identifiers:
34679
Local pid:
pubs:34679

Terms of use


Metrics



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

TO TOP