Kimiko Suto

Visual Outcomes in Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations

H. Nakanishi, S. Minoshima, K. Mizuta, 2015, Seminars in ophthalmology.

Clinical Phenotype in Ten Unrelated Japanese Patients with Mutations in the EYS Gene

S. Minoshima, Y. Hirami, Masayo Takahashi, 2014, Ophthalmic genetics.

The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients

H. Nakanishi, S. Minoshima, Y. Hirami, 2014, Journal of Human Genetics.

Novel OPN1LW/OPN1MW deletion mutations in 2 Japanese families with blue cone monochromacy

S. Minoshima, Makoto Nakamura, S. Kachi, 2016, Human Genome Variation.