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