Mizobuchi, K., Hayashi, T., Yoshitake, K., Fujinami, K., Tachibana, T., Tsunoda, K., . . . Nakano, T. (2020). Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findings. Mol Genet Genomic Med.

Mizobuchi, Kei, Takaaki Hayashi, Kazutoshi Yoshitake, Kaoru Fujinami, Toshiaki Tachibana, Kazushige Tsunoda, Takeshi Iwata, and Tadashi Nakano. "Novel Homozygous CLN3 Missense Variant in Isolated Retinal Dystrophy: A Case Report and Electron Microscopic Findings." Mol Genet Genomic Med 2020.

Mizobuchi, Kei, et al. "Novel Homozygous CLN3 Missense Variant in Isolated Retinal Dystrophy: A Case Report and Electron Microscopic Findings." Mol Genet Genomic Med 2020.