AF286472[Secondary Source ID] - Search Results

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Mutational risk in highly repetitive exon ORF15 of the RPGR multidisease gene is not associated with haplotype background.

Jacobi FK, Karra D, Broghammer M, Blin N, Pusch CM. Jacobi FK, et al. Int J Mol Med. 2005 Dec;16(6):1175-8. Int J Mol Med. 2005. PMID: 16273303

X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15.

Demirci FY, Rigatti BW, Wen G, Radak AL, Mah TS, Baic CL, Traboulsi EI, Alitalo T, Ramser J, Gorin MB. Demirci FY, et al. Am J Hum Genet. 2002 Apr;70(4):1049-53. doi: 10.1086/339620. Epub 2002 Feb 20. Am J Hum Genet. 2002. PMID: 11857109 Free PMC article.

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