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Glyceraldehyde-Derived Advanced Glycation End Products Accumulate Faster Than N(ε)-(Carboxymethyl) Lysine

Yokota M, Sekita M, Okano Y, Masaki H, Takeuchi M, Tokudome Y

No abstract available.
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Pterin & DHPR measurement and DNA analysis in Korean PKU patients

Chong CH, Lee HY, Lee DH, Lee SJ, Cha KW, Yim JB, Okano Y

  • KMID: 2208554
  • J Korean Pediatr Soc.
  • 1993 Dec;36(12):1681-1690.
Phenylketonuria is metabolic disorder that results from a deficiency of the hepatic phenylalanine hydroxylase. But among patients with hyperphenylalaninemia, the defect resides in one of the enzymes necessary for production...
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