Cite
A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD
MLA
Akiko Suga, et al. “A Homozygous Structural Variant of RPGRIP1 Is Frequently Associated with Achromatopsia in Japanese Patients with IRD.” Genetics in Medicine Open, vol. 2, no. 101843-, Jan. 2024. EBSCOhost, https://doi.org/10.1016/j.gimo.2024.101843.
APA
Akiko Suga, Kei Mizobuchi, Taiga Inooka, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kazuki Kuniyoshi, Yosuke Kawai, Yosuke Omae, Katsushi Tokunaga, Takaaki Hayashi, Shinji Ueno, Takeshi Iwata, Hatsue Ishibashi-Ueda, Tsutomu Tomita, Michio Noguchi, Ayako Takahashi, Yu-ichi Goto, Sumiko Yoshida, … Hideyuki Shimanuki. (2024). A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD. Genetics in Medicine Open, 2(101843-). https://doi.org/10.1016/j.gimo.2024.101843
Chicago
Akiko Suga, Kei Mizobuchi, Taiga Inooka, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kazuki Kuniyoshi, et al. 2024. “A Homozygous Structural Variant of RPGRIP1 Is Frequently Associated with Achromatopsia in Japanese Patients with IRD.” Genetics in Medicine Open 2 (101843-). doi:10.1016/j.gimo.2024.101843.