Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug-Reference-Cited by-同舟云学术

Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug

Published:2019-04-22 Issue:5 Volume:22 Page:700-708
ISSN:1097-6256
Container-title:Nature Neuroscience
language:en
Short-container-title:Nat Neurosci

Author:

Barak Boaz^ORCID,Zhang Zicong,Liu Yuanyuan,Nir Ariel,Trangle Sari S.,Ennis Michaela^ORCID,Levandowski Kirsten M.,Wang Dongqing,Quast Kathleen,Boulting Gabriella L.,Li Yi,Bayarsaihan Dashzeveg,He Zhigang^ORCID,Feng Guoping^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Neuroscience

Link

http://www.nature.com/articles/s41593-019-0380-9.pdf

Reference56 articles.

1. Barak, B. & Feng, G. Neurobiology of social behavior abnormalities in autism and Williams syndrome. Nat. Neurosci. 19, 647–655 (2016).

2. Pober, B. R. Williams–Beuren syndrome. N. Engl. J. Med. 362, 239–252 (2010).

3. Karmiloff-Smith, A. et al. Social cognition in Williams syndrome: genotype/phenotype insights from partial deletion patients. Front. Psychol. 3, 168 (2012).

4. Dai, L. et al. Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays. Am. J. Med. Genet. A 149A, 302–314 (2009).

5. Morris, C. A. et al. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype–phenotype analysis of five families with deletions in the Williams syndrome region. Am. J. Med. Genet. A 123A, 45–59 (2003).

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