Both authors contributed equally to this work.
Two mutations in human BICC1 resulting in Wnt pathway hyperactivity associated with cystic renal dysplasia†
Article first published online: 31 OCT 2011
© 2011 Wiley Periodicals, Inc.
Volume 33, Issue 1, pages 86–90, January 2012
How to Cite
Kraus, M. R.-C., Clauin, S., Pfister, Y., Di Maïo, M., Ulinski, T., Constam, D., Bellanné-Chantelot, C. and Grapin-Botton, A. (2012), Two mutations in human BICC1 resulting in Wnt pathway hyperactivity associated with cystic renal dysplasia. Hum. Mutat., 33: 86–90. doi: 10.1002/humu.21610
Communicated by Michel Goossens
- Issue published online: 14 DEC 2011
- Article first published online: 31 OCT 2011
- Accepted manuscript online: 15 SEP 2011 01:58PM EST
- Manuscript Accepted: 29 AUG 2011
- Manuscript Received: 8 JUL 2011
- Ecole Polytechnique Fédérale de Lausanne (to D.C. and A.G.B.)
- Swiss National Science Foundation (CRSI133_1306662 [to D.C. and A.G.B.])
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