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RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa.

Arch Ophthalmol 128(7):915-23 (2010) PMID 20625056

To assess the phenotype of patients with X-linked retinitis pigmentosa (XLRP) with RP2 mutations and to correlate the findings with their genotype.

DOI: 10.1001/archophthalmol.2010.122
Version: za2963e q8za1 q8zb4 q8zc4 q8zdc q8zed q8zf9 q8zga

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