Behavioral training rescues motor deficits in Cyfip1 haploinsufficiency mouse model of autism spectrum disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biological Psychiatry,Cellular and Molecular Neuroscience,Psychiatry and Mental health
Link
http://www.nature.com/articles/s41398-018-0338-9.pdf
Reference51 articles.
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2. Cox, D. M. & Butler, M. G. The 15q11.2 BP1-BP2 microdeletion syndrome: a review. Int. J. Mol. Sci. 16, 4068–4082 (2015).
3. Butler, M. G., Bittel, D. C., Kibiryeva, N., Talebizadeh, Z. & Thompson, T. Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy. Pediatrics 113, 565–573 (2004).
4. Bittel, D. C., Kibiryeva, N. & Butler, M. G. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome. Pediatrics 118, e1276–e1283 (2006).
5. Chen, B. et al. The WAVE regulatory complex links diverse receptors to the actin cytoskeleton. Cell 156, 195–207 (2014).
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