2 results for author:"Hirakata A." in Literature citations
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| ABCA4 gene mutations in Japanese patients with Stargardt disease and retinitis pigmentosa. Fukui T., Yamamoto S., Nakano K., Tsujikawa M., Morimura H., Nishida K., Ohguro N., Fujikado T., Irifune M., Kuniyoshi K. et al. Invest. Ophthalmol. Vis. Sci. 43:2819-2824(2002) · Mapped (8) |
| Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene. Hotta Y., Fujiki K., Hayakawa M., Ohta T., Fujimaki T., Tamaki K., Yokoyama T., Kanai A., Hirakata A., Hida T. et al. Hum. Genet. 103:142-144(1998) · UniProtKB (1) |