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Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15

  • Author(s): Demirci, FYK
  • Gupta, N
  • Radak, AL
  • Rigatti, BW
  • Mah, TS
  • Milam, AH
  • Gorin, MB
  • et al.
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