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RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa
- Correspondence to: Dr Serge Amselem INSERM U. 654 Hôpital Henri-Mondor, 51, avenue du Maréchal de Lattre-de-Tassigny, 94010 Créteil cedex, France; serge.amselem{at}im3.inserm.fr
Citation
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa
Publication history
- Accepted July 25, 2005
- Revised July 22, 2005
- First published July 31, 2005.
Online issue publication
November 10, 2016
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Copyright 2006 Journal of Medical Genetics