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
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