Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation
2014 ◽
Vol 1844
(12)
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pp. 2355-2365
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1991 ◽
Vol 90
(2)
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pp. 179-188
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1987 ◽
Vol 10
(4)
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pp. 330-338
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