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Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation by Xiulan Lu, Xiulan Lu, Weijian Chen, Weijian Chen, Liping Li, Xinyuan Zhu, Caizhi Huang, Saijun Liu, Yongjia Yang, Yaowang Zhao, Yaowang Zhao
Published 2019Connect to this object online.
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