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Disease: Cone dystrophy- x-linked- with tapetal-like sheen

  • Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree
  • Clinical utility gene card for: achromatopsia
  • Clinical utility gene card for: blue cone monochromatism
  • X-linked cone dystrophy with an uncommon tapetal-like sheen caused by a novel RPGR variant
  • X-linked progressive cone dystrophy. Clinical characteristics of affected males and female carriers
  • X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenon
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