Article info
New disease loci
Short report
Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18)
- Correspondence to Professor Helene Dollfus, Faculté de Médecine, Université de Strasbourg, Laboratoire de Génétique Médicale, INSERM 1112, Faculté de Médecine, Bâtiment 3, 11 rue Humann, Strasbourg 67085, France; dollfus{at}unistra.fr
Citation
Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18)
Publication history
- Received April 26, 2013
- Revised July 27, 2013
- Accepted August 16, 2013
- First published September 11, 2013.
Online issue publication
January 20, 2014
Article Versions
- Previous version (11 September 2013).
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