Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome
暂无分享,去创建一个
J. Kira | S. Tsujino | Y. Eto | T. Yamada | T. Ohashi | N. Kanazawa | T. Saito | Takeshi Yamada | Toyokazu Saito | Tohya Ohashi