Journal article
Anxious, hypoactive phenotype combined with motor deficits in Gtf2ird1 null mouse model relevant to Williams syndrome.
- Abstract:
-
Williams-Beuren syndrome (WBS) is a rare genetic disorder caused by a hemizygous deletion of around 28 genes on the long arm of chromosome 7 (7q11.23), characterized by a unique spectrum of behavioral impairments, including mental retardation, deficits in visuospatial constructive cognition, hypersociability, anxiety and simple phobias. Physical characteristics include dysmorphic faces, short stature, oculomotor deficits, gross and fine coordination impairments, diminished control of balance ...
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- Publication status:
- Published
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- Publisher copy:
- 10.1016/j.bbr.2012.05.014
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Bibliographic Details
- Journal:
- Behavioural brain research
- Volume:
- 233
- Issue:
- 2
- Pages:
- 458-473
- Publication date:
- 2012-08-01
- DOI:
- EISSN:
-
1872-7549
- ISSN:
-
0166-4328
- Source identifiers:
-
334712
Item Description
- Language:
- English
- Keywords:
- Pubs id:
-
pubs:334712
- UUID:
-
uuid:7fc5f5bc-2c38-4736-a2fa-9d09ee87a10f
- Local pid:
- pubs:334712
- Deposit date:
- 2012-12-19
Terms of use
- Copyright date:
- 2012
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