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

Kazuma Oku, Kei Mizobuchi, Kiyofumi Mochizuki, Kazushige Tsunoda, Itsuka Matsushita, Tatsuo Nagata, Kaoru Fujinami, Akiko Suga, Kazutoshi Yoshitake, Hirokazu Sakaguchi, Takaaki Hayashi, Takeshi Iwata, Hiroyuki Kondo