Mutations in CIB2 calcium and integrin-binding protein disrupt auditory hair cell calcium homeostasis in Usher syndrome type 1J and non-syndromic deafness DFNB48
Version of Record online: 12 MAR 2013
© 2013 John Wiley & Sons A/S. Published by Blackwell Publishing Ltd
Volume 83, Issue 4, pages 317–318, April 2013
How to Cite
Jan, A. (2013), Mutations in CIB2 calcium and integrin-binding protein disrupt auditory hair cell calcium homeostasis in Usher syndrome type 1J and non-syndromic deafness DFNB48. Clinical Genetics, 83: 317–318. doi: 10.1111/cge.12100
- Issue online: 12 MAR 2013
- Version of Record online: 12 MAR 2013
- Accepted manuscript online: 18 JAN 2013 01:10PM EST
- Manuscript Accepted: 14 JAN 2013
- Manuscript Revised: 7 JAN 2013
- Manuscript Received: 28 NOV 2012
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