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An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene
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  1. Correspondence to: Dr A Webster Division of Molecular Genetics, 11–43 Bath Street, Institute of Ophthalmology, University College London, London EC1V 9EL, UK; Andrew.websterucl.ac.uk
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Citation

Dandekar SS, Ebenezer ND, Grayson C, et al
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene

Publication history

  • Accepted September 5, 2003
  • First published March 18, 2004.
Online issue publication 
March 18, 2004

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