1. A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD
- Author
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Suga, Akiko, primary, Mizobuchi, Kei, additional, Inooka, Taiga, additional, Yoshitake, Kazutoshi, additional, Minematsu, Naoko, additional, Tsunoda, Kazushige, additional, Kuniyoshi, Kazuki, additional, Kawai, Yosuke, additional, Omae, Yosuke, additional, Tokunaga, Katsushi, additional, Ishibashi-Ueda, Hatsue, additional, Tomita, Tsutomu, additional, Noguchi, Michio, additional, Takahashi, Ayako, additional, Goto, Yu-ichi, additional, Yoshida, Sumiko, additional, Hattori, Kotaro, additional, Matsumura, Ryo, additional, Iida, Aritoshi, additional, Maruoka, Yutaka, additional, Gatanaga, Hiroyuki, additional, Sugiyama, Masaya, additional, Suzuki, Satoshi, additional, Miyo, Kengo, additional, Matsubara, Yoichi, additional, Umezawa, Akihiro, additional, Hata, Kenichiro, additional, Kaname, Tadashi, additional, Ozaki, Kouichi, additional, Tokuda, Haruhiko, additional, Watanabe, Hiroshi, additional, Niida, Shumpei, additional, Noiri, Eisei, additional, Kitajima, Koji, additional, Miyahara, Reiko, additional, Shimanuki, Hideyuki, additional, Hayashi, Takaaki, additional, Ueno, Shinji, additional, and Iwata, Takeshi, additional
- Published
- 2024
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