Rchr

J-GLOBAL ID：200901069073507608 Update date: Aug. 29, 2020

Itabashi Toshitaka

イタバシトシタカ | Itabashi Toshitaka

Affiliation and department：
Job title： Research Associate
Research theme for competitive and other funds (2)：

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MISC (24)：

H Sato, Y Wada, T Itabashi, M Nakamura, M Kawamura, M Tamai. Mutations in the Pre-mRNA splicing gene, PRPF31, in Japanese families with autosomal dominant retinitis pigmentosa. AMERICAN JOURNAL OF OPHTHALMOLOGY. 2005. 140. 3. 537-540
H Sato, Y Wada, T Itabashi, M Nakamura, M Kawamura, M Tamai. Mutations in the Pre-mRNA splicing gene, PRPF31, in Japanese families with autosomal dominant retinitis pigmentosa. AMERICAN JOURNAL OF OPHTHALMOLOGY. 2005. 140. 3. 537-540
Y Wada, A Tada, T Itabashi, M Kawamura, H Sato, M Tamai. Screening for mutations in the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa. AMERICAN JOURNAL OF OPHTHALMOLOGY. 2005. 140. 1. 163-165
Y Wada, A Tada, T Itabashi, M Kawamura, H Sato, M Tamai. Screening for mutations in the IMPDH1 gene in Japanese patients with autosomal dominant retinitis pigmentosa. AMERICAN JOURNAL OF OPHTHALMOLOGY. 2005. 140. 1. 163-165
Y Wada, T Itabashi, H Sato, M Kawamura, A Tada, M Tamai. Screening for mutations in CYP4V2 gene in Japanese patients with Bietti's crystalline corneoretinal dystrophy. AMERICAN JOURNAL OF OPHTHALMOLOGY. 2005. 139. 5. 894-899

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