Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa.

Published in:

PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0108721

By:

• Katagiri, Satoshi;
• Akahori, Masakazu;
• Sergeev, Yuri;
• Yoshitake, Kazutoshi;
• Ikeo, Kazuho;
• Furuno, Masaaki;
• Hayashi, Takaaki;
• Kondo, Mineo;
• Ueno, Shinji;
• Tsunoda, Kazushige;
• Shinoda, Kei;
• Kuniyoshi, Kazuki;
• Tsurusaki, Yohinori;
• Matsumoto, Naomichi;
• Tsuneoka, Hiroshi;
• Iwata, Takeshi

Publication type:

Article