Two Novel AGXT Mutations Cause the Infantile Form of...

Frontiers in Pharmacology 2019 / 2 Vol. 10

Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation

Lu, Xiulan, Chen, Weijian, Li, Liping, Zhu, Xinyuan, Huang, Caizhi, Liu, Saijun, Yang, Yongjia, Zhao, Yaowang
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Volume:
10
Language:
english
Journal:
Frontiers in Pharmacology
DOI:
10.3389/fphar.2019.00085
Date:
February, 2019
File:
PDF, 5.10 MB
english, 2019
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