Author:
Frye Richard E.,Cox Devin,Slattery John,Tippett Marie,Kahler Stephen,Granpeesheh Doreen,Damle Shirish,Legido Agustin,Goldenthal Michael J.
Publisher
Springer Science and Business Media LLC
Reference44 articles.
1. Phelan, K. & McDermid, H. E. The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome). Mol. Syndromol. 2, 186–201 (2012).
2. Peca, J. et al. Shank3 mutant mice display autistic-like behaviours and striatal dysfunction. Nature 472, 437–442 (2011).
3. Disciglio, V. et al. Interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndrome. Am. J. Med. Genet. 164, 1666–1676 (2014).
4. Frye, R. E. Mitochondrial disease in 22q13 duplication syndrome. J. Child. Neurol. 27, 942–949 (2012).
5. Ton, C., Hwang, D. M., Dempsey, A. A. & Liew, C. C. Identification and primary structure of five human NADH-ubiquinone oxidoreductase subunits. Biochem. Biophys. Res. Commun. 241, 589–594 (1997).
Cited by
44 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献