How to Cite this Article: de Leeuw N, Bulk S, Green A, Jaeckle-Santos L, Baker LA, Zinn AR, Kleefstra T, van der Smagt JJ, Vianne Morgante AM, de Vries BBA, van Bokhoven H, de Brouwer APM. 2010. UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients. Am J Med Genet Part A 152A:3084–3090.
UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients†
Version of Record online: 24 NOV 2010
Copyright © 2010 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 152A, Issue 12, pages 3084–3090, December 2010
How to Cite
de Leeuw, N., Bulk, S., Green, A., Jaeckle-Santos, L., Baker, L. A., Zinn, A. R., Kleefstra, T., van der Smagt, J. J., Vianne Morgante, A. M., de Vries, B. B.A., van Bokhoven, H. and de Brouwer, A. P.M. (2010), UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients. Am. J. Med. Genet., 152A: 3084–3090. doi: 10.1002/ajmg.a.33743
- Issue online: 24 NOV 2010
- Version of Record online: 24 NOV 2010
- Manuscript Accepted: 6 SEP 2010
- Manuscript Received: 15 JUN 2010
- UT Southwestern Medical School
- Dutch Organisation for Health Research and Development. Grant Number: ZON-MW 917-86-319
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