A mutation in CRX causing pigmented paravenous retinochoroidal atrophy.
Jin Kyun OhYan NuzbrokhWinston LeeJose Ronaldo Lima de CarvalhoNan Kai WangJanet R SparrowRando AllikmetsStephen H TsangPublished in: European journal of ophthalmology (2020)
This case report broadens the currently known phenotypic presentations of CRX-associated retinopathy and suggests that mutations in CRX may be associated with pigmented paravenous retinochoroidal atrophy.
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