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Article

Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene.

Translational vision science & technology - 1 Jun 2021

Kondo Hiroyuki, Matsushita Itsuka, Nagata Tatsuo, Fujihara Etsuko, Hosono Katsuhiro, Uchio Eiichi, Hotta Yoshihiro, Kusaka Shunji

Abstract excerpt

Purpose: To determine the clinical characteristics of patients and family members with familial exudative vitreoretinopathy (FEVR) caused by mutations in the KIF11 gene. Methods: Twenty-one patients from 10 FEVR families with mutations in the KIF11 gene were studied. The retinal and systemic features were examined. The genetic analyses performed included Sanger sequencing of the KIF11 gene, whole exome...

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Identifiers

PMID: 34128965
DOI: 10.1167/tvst.10.7.18
PMCID: PMC8212440

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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