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