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Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.

Abstract:

Mental retardation affects 2-3% of the population and shows a high heritability.Neurodevelopmental disorders that include pronounced impairment in language and speech skills occur less frequently. For most cases, the molecular basis of mental retardation with or without speech and language disorder is unknown due to the heterogeneity of underlying genetic factors.We have used molecular karyotyping on 1523 patients with mental retardation to detect copy number variations (CNVs) including delet...

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Publication status:
Published

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Publisher copy:
10.1002/humu.21362

Authors


Kapeller, J More by this author
Rivera-Brugués, N More by this author
Lorenz-Depiereux, B More by this author
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Journal:
Human mutation
Volume:
31
Issue:
11
Pages:
E1851-E1860
Publication date:
2010-11-05
DOI:
EISSN:
1098-1004
ISSN:
1059-7794
URN:
uuid:b6993216-09c6-4079-988b-fdb8149821a1
Source identifiers:
94604
Local pid:
pubs:94604

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