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Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissues

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Journal of Inherited Metabolic Disease

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References

  • Terheggen, H. G., Schwenk, A., Lowenthal, A., van Sande, M. and Colombo, J. P. Argininaemia with arginase deficiency.Lancet 2 (1969) 748–749

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  • Walser, M. Urea cycle disorders and other hereditary hyperammonemic syndromes. In Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M.S. (eds.)The Metabolic Basis of Inherited Disease, 5th Edn. McGraw-Hill, New York, 1983, pp. 402–438

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Authors and Affiliations

  1. Children's Hospital, University of Munich, Germany

    W. Endres, R. Schaller & Y. S. Shin

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  1. W. Endres
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  2. R. Schaller
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  3. Y. S. Shin
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Endres, W., Schaller, R. & Shin, Y.S. Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissues. J Inherit Metab Dis 7, 8 (1984). https://doi.org/10.1007/BF01805610

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  • DOI: https://doi.org/10.1007/BF01805610

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