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A decrease in glycine cleavage activity in the liver of a patient with dihydrolipoyl dehydrogenase deficiency

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Journal of Inherited Metabolic Disease

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References

  • Hayasaka, K., Narisawa, K., Satoh, T., Tateda, H., Metoki, K., Tada, K., Hiraga, K., Aoki, T., Kawakami, T., Akamatsu, H. and Matsuo, N. Glycine cleavage system in ketotic hyperglycinemia: a reduction of H-protein activity.Pediatr. Res. 16 (1982) 5–7

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  • Matsuda, S., Kitano, A., Sakaguchi, Y., Yoshino, M. and Saheki, T. Pyruvate dehydrogenase subcomplex with lipoamide dehydrogenase deficiency in a patient with lactic acidosis and branched chain ketoaciduria.Clin. Chim. Acta 140 (1984) 59–64

    Google Scholar 

  • Sakaguchi, Y., Yoshino, M., Aramaki, S., Yoshida, I., Yamashita, F., Kuhara, T., Matsumoto, I. and Hayashi, T. Dihydrolipoyl dehydrogenase deficiency: a therapeutic trial with branched-chain amino acid restriction.Eur. J. Pediatr. 145 (1986)271–274

    Google Scholar 

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Authors and Affiliations

  1. From: Department of Paediatrics, Kurume University School of Medicine, 830, Kurume, Japan

    M. Yoshino, Y. Koga & F. Yamashita

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  1. M. Yoshino
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  2. Y. Koga
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  3. F. Yamashita
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Yoshino, M., Koga, Y. & Yamashita, F. A decrease in glycine cleavage activity in the liver of a patient with dihydrolipoyl dehydrogenase deficiency. J Inherit Metab Dis 9, 399–400 (1986). https://doi.org/10.1007/BF01800493

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  • DOI: https://doi.org/10.1007/BF01800493

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