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2016
H. Bardak, Gunay, M., Yildiz, E., Bardak, Y., Gunay, B., Ozbas, H., and Bagci, O., Novel visual system homeobox 1 gene mutations in Turkish patients with keratoconus, vol. 15, no. 4, p. -, 2016.
Conflicts of interestThe authors declare no conflict of interest.REFERENCESAbu-Amero KK, Kalantan H, Al-Muammar AM, et al (2011). Analysis of the VSX1 gene in keratoconus patients from Saudi Arabia. Mol. Vis. 17: 667-672. Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, et al (2010). A method and server for predicting damaging missense mutations. Nat. Methods 7: 248-249. http://dx.doi.org/10.1038/nmeth0410-248 Arnal E, Peris-Martínez C, Menezo JL, Johnsen-Soriano S, et al (2011). Oxidative stress in keratoconus? Invest. Ophthalmol. Vis. Sci. 52: 8592-8597. http://dx.doi.org/10.1167/iovs.11-7732 Atilano SR, Coskun P, Chwa M, Jordan N, et al (2005). Accumulation of mitochondrial DNA damage in keratoconus corneas. Invest. Ophthalmol. Vis. Sci. 46: 1256-1263. http://dx.doi.org/10.1167/iovs.04-1395 Bamshad MJ, Ng SB, Bigham AW, Tabor HK, et al (2011). Exome sequencing as a tool for Mendelian disease gene discovery. Nat. Rev. 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