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Clinical features of a Japanese case with Bothnia dystrophy.
Nojima K, Hosono K, Zhao Y, Toshiba T, Hikoya A, Asai T, Kato M, Kondo M, Minoshima S, Hotta Y. Nojima K, et al. Among authors: hikoya a. Ophthalmic Genet. 2012 Jun;33(2):83-8. doi: 10.3109/13816810.2011.634877. Epub 2011 Dec 15. Ophthalmic Genet. 2012. PMID: 22171637
Three novel mutations of the PAX6 gene in Japanese aniridia patients.
Kawano T, Wang C, Hotta Y, Sato M, Iwata-Amano E, Hikoya A, Fujita N, Koyama N, Shirai S, Azuma N, Ohtsubo M, Shimizu N, Minoshima S. Kawano T, et al. Among authors: hikoya a. J Hum Genet. 2007;52(7):571-574. doi: 10.1007/s10038-007-0153-2. Epub 2007 Jun 14. J Hum Genet. 2007. PMID: 17568989
Central corneal thickness in Japanese children.
Hikoya A, Sato M, Tsuzuki K, Koide YM, Asaoka R, Hotta Y. Hikoya A, et al. Jpn J Ophthalmol. 2009 Jan;53(1):7-11. doi: 10.1007/s10384-008-0619-6. Epub 2009 Jan 30. Jpn J Ophthalmol. 2009. PMID: 19184302
A case of aniridia with unilateral Peters anomaly.
Sawada M, Sato M, Hikoya A, Wang C, Minoshima S, Azuma N, Hotta Y. Sawada M, et al. Among authors: hikoya a. J AAPOS. 2011 Feb;15(1):104-6. doi: 10.1016/j.jaapos.2010.11.006. J AAPOS. 2011. PMID: 21397818
35 results