Title : Successful outcome after early combined liver and en bloc-kidney transplant in an infant with primary hyperoxaluria type 1: a case report.

Pub. Date : 2009 Nov

PMID : 19496983






1 Functional Relationships(s)
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1 PH1 is a metabolic disorder characterized by urolithiasis and the accumulation of oxalate crystals in the kidneys and other organs. Oxalates alanine--glyoxylate and serine--pyruvate aminotransferase Homo sapiens