Both the authors contributed equally to this work
Mesoaxial polydactyly is a major feature in Bardet–Biedl syndrome patients with LZTFL1 (BBS17) mutations
Article first published online: 12 JUN 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 5, pages 476–481, May 2014
How to Cite
Schaefer, E., Lauer, J., Durand, M., Pelletier, V., Obringer, C., Claussmann, A., Braun, J.-J., Redin, C., Mathis, C., Muller, J., Schmidt-Mutter, C., Flori, E., Marion, V., Stoetzel, C. and Dollfus, H. (2014), Mesoaxial polydactyly is a major feature in Bardet–Biedl syndrome patients with LZTFL1 (BBS17) mutations. Clinical Genetics, 85: 476–481. doi: 10.1111/cge.12198
- Issue published online: 1 APR 2014
- Article first published online: 12 JUN 2013
- Accepted manuscript online: 21 MAY 2013 12:14PM EST
- Manuscript Revised: 16 MAY 2013
- Manuscript Accepted: 16 MAY 2013
- Manuscript Received: 6 FEB 2013
- RETINA France
- UNADEV (Union Nationale des Aveugles et Déficients Visuels)
- PHRC (Programme Hospitalier pour la Recherche Clinique) program
- Agence Nationale pour la Recherche GENOPATH
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