التفاصيل البيبلوغرافية
| العنوان: |
A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD |
| المؤلفون: |
Ishibashi-Ueda, Hatsue, Tomita, Tsutomu, Noguchi, Michio, Takahashi, Ayako, Goto, Yu-ichi, Yoshida, Sumiko, Hattori, Kotaro, Matsumura, Ryo, Iida, Aritoshi, Maruoka, Yutaka, Gatanaga, Hiroyuki, Sugiyama, Masaya, Suzuki, Satoshi, Miyo, Kengo, Matsubara, Yoichi, Umezawa, Akihiro, Hata, Kenichiro, Kaname, Tadashi, Ozaki, Kouichi, Tokuda, Haruhiko, Watanabe, Hiroshi, Niida, Shumpei, Noiri, Eisei, Kitajima, Koji, Omae, Yosuke, Miyahara, Reiko, Shimanuki, Hideyuki, Kawai, Yosuke, Tokunaga, Katsushi, Suga, Akiko, Mizobuchi, Kei, Inooka, Taiga, Yoshitake, Kazutoshi, Minematsu, Naoko, Tsunoda, Kazushige, Kuniyoshi, Kazuki, Hayashi, Takaaki, Ueno, Shinji, Iwata, Takeshi |
| المصدر: |
In Genetics in Medicine Open 2024 2 |
| قاعدة البيانات: |
ScienceDirect |
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