Communicated by Sergio Ottolenghi
A p.D116G mutation in CREB1 leads to novel multiple malformation syndrome resembling CrebA knockout mouse†
Version of Record online: 14 FEB 2012
© 2012 Wiley Periodicals, Inc.
Special Issue: Focus on the NIH Undiagnosed Diseases Program
Volume 33, Issue 4, pages 651–654, April 2012
How to Cite
Kitazawa, S., Kondo, T., Mori, K., Yokoyama, N., Matsuo, M. and Kitazawa, R. (2012), A p.D116G mutation in CREB1 leads to novel multiple malformation syndrome resembling CrebA knockout mouse. Hum. Mutat., 33: 651–654. doi: 10.1002/humu.22027
- Issue online: 12 MAR 2012
- Version of Record online: 14 FEB 2012
- Accepted manuscript online: 20 JAN 2012 12:00AM EST
- Manuscript Accepted: 4 JAN 2012
- Manuscript Received: 28 JUN 2011
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