A decrease in glycine cleavage activity in the liver of a patient with dihydrolipoyl dehydrogenase deficiency
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01800493
Reference3 articles.
1. 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
2. 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
3. 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
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