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RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa.
Jayasundera T, Branham KE, Othman M, Rhoades WR, Karoukis AJ, Khanna H, Swaroop A, Heckenlively JR. Jayasundera T, et al. Among authors: othman m. Arch Ophthalmol. 2010 Jul;128(7):915-23. doi: 10.1001/archophthalmol.2010.122. Arch Ophthalmol. 2010. PMID: 20625056 Free PMC article.
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.
Friedman JS, Chang B, Kannabiran C, Chakarova C, Singh HP, Jalali S, Hawes NL, Branham K, Othman M, Filippova E, Thompson DA, Webster AR, Andréasson S, Jacobson SG, Bhattacharya SS, Heckenlively JR, Swaroop A. Friedman JS, et al. Among authors: othman m. Am J Hum Genet. 2006 Dec;79(6):1059-70. doi: 10.1086/510021. Epub 2006 Oct 23. Am J Hum Genet. 2006. PMID: 17186464 Free PMC article.
Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.
Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Roman AJ, Windsor EA, Steinberg JD, Branham K, Othman M, Swaroop A, Jacobson SG. Aleman TS, et al. Among authors: othman m. Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4759-65. doi: 10.1167/iovs.07-0453. Invest Ophthalmol Vis Sci. 2007. PMID: 17898302 Free PMC article.
1,094 results