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Article

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

Seminars in ophthalmology - 1 Jan 2018

Nagase Yasunori, Kurata Kentaro, Hosono Katsuhiro, Suto Kimiko, Hikoya Akiko, Nakanishi Hiroshi, Mizuta Kunihiro, Mineta Hiroyuki, Minoshima Shinsei, Hotta Yoshihiro

Abstract excerpt

PURPOSE: EYS and USH2A are the most common causative genes for retinitis pigmentosa (RP) in Japan. We determined the clinical outcomes for USH2A-related non-syndromic RP or Usher syndrome type II (USH2). METHODS: Two non-syndromic RP and 11 USH2 patients with previously identified USH2A mutations were included. Their complete history and medical records were collected using standard procedures. Visual fields and...

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Identifiers

PMID: 28678594
DOI: 10.1080/08820538.2017.1340487

Genes

EYS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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