Toshitaka Itabashi

Screening for Mutations in CYP4V2 Gene in Japanese Patients With Bietti’s Crystalline Corneoretinal Dystrophy

Yuko Wada, Toshitaka Itabashi, Hajime Sato et al. · American Journal of Ophthalmology · 2005 · 58 citations

Mendelian Disorder, Genetic Disorder, Genetics +5

Mutations in the Pre-mRNA Splicing Gene, PRPF31, in Japanese Families With Autosomal Dominant Retinitis Pigmentosa

Hajime Sato, Yuko Wada, Toshitaka Itabashi et al. · American Journal of Ophthalmology · 2005 · 34 citations

Rna Processing, Systems Biology, Genetic Disorder +9

Screening of the MERTK gene for mutations in Japanese patients with autosomal recessive retinitis pigmentosa.

A. Tada, Yuko Wada, Hajime Sato et al. · PubMed · 2006 · 30 citations

Novel 615delC mutation in the CRX gene in a Japanese family with cone-rod dystrophy

Toshitaka Itabashi, Yuko Wada, Hajime Sato et al. · American Journal of Ophthalmology · 2004 · 19 citations

Mendelian Disorder, Crx Gene, Genetic Disorder +9

Novel 2336-2337delCT mutation in RP1 gene in a japanese family with autosomal dominant retinitis pigmentosa

Miyuki Kawamura, Yuko Wada, Yoshihiro Noda et al. · American Journal of Ophthalmology · 2004 · 17 citations

Novel 2336-2337Delct Mutation, Mendelian Disorder, Genetic Disorder +9