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RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections
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  1. Correspondence to:
 Dr A J Hardcastle, Division of Molecular Genetics, Institute of Ophthalmology, University College London, 11-43 Bath Street, London EC1V 9EL, UK; 
 a.hardcastle{at}ucl.ac.uk
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Citation

Zito I, Downes SM, Patel RJ, et al
RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections

Publication history

  • First published August 14, 2003.
Online issue publication 
August 14, 2003

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