These authors contributed equally to the paper.
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)
Article first published online: 27 MAR 2014
© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 87, Issue 3, pages 252–258, March 2015
How to Cite
Banka, S., Lederer, D., Benoit, V., Jenkins, E., Howard, E., Bunstone, S., Kerr, B., McKee, S., Lloyd, I.C., Shears, D., Stewart, H., White, S.M., Savarirayan, R., Mancini, G.M.S., Beysen, D., Cohn, R.D., Grisart, B., Maystadt, I. and Donnai, D. (2015), Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2). Clinical Genetics, 87: 252–258. doi: 10.1111/cge.12363
The authors declare no conflict of interest.
- Issue published online: 12 FEB 2015
- Article first published online: 27 MAR 2014
- Accepted manuscript online: 14 FEB 2014 09:40AM EST
- Manuscript Accepted: 12 FEB 2014
- Manuscript Revised: 9 FEB 2014
- Manuscript Received: 2 JAN 2014
- Central Manchester University Hospitals NHS Foundation Trust. Grant Number: 629396
|cge12363-sup-0001-AppendixS1.docx||Word 2007 document||3578K||Appendix S1. Clinical description and mutation analysis of seven patients.|
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