These authors have equally contributed.
Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis
Version of Record online: 5 APR 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 2, pages 172–177, February 2014
How to Cite
M'hamdi, O., Redin, C., Stoetzel, C., Ouertani, I., Chaabouni, M., Maazoul, F., M'rad, R., Mandel, J.L., Dollfus, H., Muller, J. and Chaabouni, H. (2014), Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis. Clinical Genetics, 85: 172–177. doi: 10.1111/cge.12129
The authors have reported no conflicts of interest.
- Issue online: 13 JAN 2014
- Version of Record online: 5 APR 2013
- Accepted manuscript online: 21 FEB 2013 03:49PM EST
- Manuscript Revised: 18 FEB 2013
- Manuscript Accepted: 18 FEB 2013
- Manuscript Received: 16 AUG 2012
- Agence de Biomedicine France
- Association Française contre les myopathies (AFM)
- Ministry of High Education and Scientific Research and Technology
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