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    Br J Ophthalmol. 2005 Aug;89(8):1065-6.

    An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome.

    Chavala SH, Sari A, Lewis H, Pauer GJ, Simpson E, Hagstrom SA, Traboulsi EI.

    PMID: 16024868 [PubMed - indexed for MEDLINE]

    PMCID: 1772771

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