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Primary hyperoxaluria type I (PH1) is an autosomal recessive disease characterized by excessive oxalate production by hepatocytes due to the deficiency of peroxisomal alanine-glyoxylate aminotransferase (AGT) activity,
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Document Date: 2012-02-21 11:23:03
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Primary hyperoxaluria type I (PH1) is an autosomal recessive disease characterized by excessive oxalate production by hepatocytes due to the deficiency of peroxisomal alanine-glyoxylate aminotransferase (AGT) activity,