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. 1999 Apr;64(4):1210–1215. doi: 10.1086/302325

Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study.

A J Hardcastle, D L Thiselton, L Van Maldergem, B K Saha, M Jay, C Plant, R Taylor, A C Bird, S Bhattacharya

PMCID: PMC1377846 PMID: 10090907

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