Primary Hyperoxaluria in Korean Pediatric Patients
Background Primary hyperoxaluria (PH), a rare inborn error of glyoxylate meta bolism causing overproduction of oxalate, is classified into three genetic subgroups: type 1-3 (PH1-PH3) caused by AGXT, GRHPR, and HOGA1 gene mutations, respectively. We performed a retrospective case series study of Kore...
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Materiálatiipa: | Girji |
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Korean Society of Pediatric Nephrology,
2019-10-01T00:00:00Z.
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