Citrin deficiency
Author:
Publisher
Springer Netherlands
Link
http://link.springer.com/content/pdf/10.1007/978-94-010-0159-5_4
Reference48 articles.
1. Saheki T, Ueda A, Hosoya M, Kusumi K, Takada S, Tsuda M and Katsunuma T. Qualitative and quantitative abnormalities of argininosuccinate synthetase in citrullinemia. Clin Chim Acta 1981; 109: 325–335.
2. Saheki T, Ueda A, Iizima K, Yamada N, Kobayashi K, Takahashi K and Katsunuma T. Argininosuccinate synthetase activity in cultured skin fibroblasts of citrullinemic patients. Clin Chim Acta 1982; 118: 93–97.
3. Saheki T, Ueda A, Hosoya M, Sase M, Nakano K and Katsunuma T. Enzymatic analysis of citrullinemia (12 cases) in Japan. Adv Exp Med Biol 1983; 153: 63–76.
4. Saheki T, Kobayashi K and Inoue I. Hereditary disorders of the urea cycle in man: biochemical and molecular approaches. Rev Physiol Biochem Pharmacol 1987; 108: 21–68.
5. Sase M, Kobayashi K, Imamura Y, Saheki T, Nakano K, Miura S and Mori M. Level of translatable messenger RNA coding for argininosuccinate synthetase in the liver of the patients with quantitative-type citrullinemia. Hum Genet 1985; 69: 130–134.
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