Yuko Wada
Department of Ophthalmology
Tohoku University School of Medicine
Sendai
Japan
Name/email consistency: high
- Screening for mutations in CYP4V2 gene in Japanese patients with Bietti's crystalline corneoretinal dystrophy. Wada, Y., Itabashi, T., Sato, H., Kawamura, M., Tada, A., Tamai, M. Am. J. Ophthalmol. (2005)
- Screening for mutations in the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa. Wada, Y., Tada, A., Itabashi, T., Kawamura, M., Sato, H., Tamai, M. Am. J. Ophthalmol. (2005)
- Clinical features of a Japanese family with autosomal dominant retinitis pigmentosa associated with a Thr494Met mutation in the HPRP3 gene. Wada, Y., Itabashi, T., Sato, H., Tamai, M. Graefes Arch. Clin. Exp. Ophthalmol. (2004)
- Autosomal dominant macular degeneration associated with 208delG mutation in the FSCN2 gene. Wada, Y., Abe, T., Itabashi, T., Sato, H., Kawamura, M., Tamai, M. Arch. Ophthalmol. (2003)
- A novel Gly35Ser mutation in the RDH5 gene in a Japanese family with fundus albipunctatus associated with cone dystrophy. Wada, Y., Abe, T., Sato, H., Tamai, M. Arch. Ophthalmol. (2001)
- Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosa. Wada, Y., Abe, T., Takeshita, T., Sato, H., Yanashima, K., Tamai, M. Invest. Ophthalmol. Vis. Sci. (2001)
- A new Leu253Arg mutation in the RP2 gene in a Japanese family with X-linked retinitis pigmentosa. Wada, Y., Nakazawa, M., Abe, T., Tamai, M. Invest. Ophthalmol. Vis. Sci. (2000)
- A frequent 1085delC/insGAAG mutation in the RDH5 gene in Japanese patients with fundus albipunctatus. Wada, Y., Abe, T., Fuse, N., Tamai, M. Invest. Ophthalmol. Vis. Sci. (2000)
