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

Overview of attention for article published in Frontiers in Pharmacology, February 2019

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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 https://t.co/DMuLZ6Oe6D #pharmacology #openaccess

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