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RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa
  1. 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
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Citation

Moore A, Escudier E, Roger G, et al
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 
March 31, 2006

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