Communicated by Dvorah Abeliovich
Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding†
Version of Record online: 28 JAN 2008
© 2008 Wiley-Liss, Inc.
Special Issue: Focus on Pharmacogenetics
Volume 29, Issue 4, pages 545–554, April 2008
How to Cite
Collin, R. W.J., Chellappa, R., Pauw, R.-J., Vriend, G., Oostrik, J., van Drunen, W., Huygen, P. L., Admiraal, R., Hoefsloot, L. H., Cremers, F. P.M., Xiang, M., Cremers, C. W.R.J. and Kremer, H. (2008), Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding. Hum. Mutat., 29: 545–554. doi: 10.1002/humu.20693
- Issue online: 10 MAR 2008
- Version of Record online: 28 JAN 2008
- Manuscript Accepted: 6 NOV 2007
- Manuscript Received: 23 MAY 2007
- Heinsius Houbolt Foundation
- European Commission FP6 Integrated Project EUROHEAR. Grant Number: LSHG-CT-20054-512063
- National Institutes of Health. Grant Numbers: EY12020, EY015777
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