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Samples in periodicals archive:
Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome.
Primary hyperoxaluria type 1 (PH1)  (OMIM 259900) is an autosomal recessive disorder of glyoxylate metabolism caused by deficiency of alanine:glyoxylate aminotransferase (AGT; EC 2.
Primary hyperoxaluria type 1 (PH1; OMIM 259900) is a rare autosomal recessive disorder characterized by impaired hepatic detoxification of glyoxylate.