Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene

Graefe s Archive for Clinical and Experimental Ophthalmology 2026

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Authors: Kazuma Oku, Kei Mizobuchi, Kiyofumi Mochizuki, Kazushige Tsunoda, Itsuka Matsushita, Tatsuo Nagata, Kaoru Fujinami, Akiko Suga, Kazutoshi Yoshitake, Hirokazu Sakaguchi, Takaaki Hayashi, Takeshi Iwata
+1 more Hiroyuki Kondo
DOI: 10.1007/s00417-025-07107-x
Cited by: 0
References: 25

Fields of Study & Subjects

Retinal Development and Disorders Retinal Diseases and Treatments Genomics and Rare Diseases

Publication details

Journal / source
Graefe s Archive for Clinical and Experimental Ophthalmology
Volume
264
Issue
5
Pages
1373–1382
Publication date
16 January 2026
Language
EN