A Ichiyama1, T Oda, E Maeda-Nakai
1First Department of Biochemistry, Hamamatsu University School of Medicine, 3600 Handa-cho, Hamamatsu, Shizuoka 431-3192, Japan. ichiyama@hama-med.ac.jp
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Primary hyperoxaluria type 1 (PH1) involves impaired serine:pyruvate/alanine:glyoxylate aminotransferase (SPT/AGT) function. Japanese PH1 patients exhibit milder symptoms, potentially linked to dietary habits influencing SPT/AGT localization.
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