References
Carson, N. A. J. Non-ketotic hyperglycinaemia — a review of 70 patients.J. Inher. Metab. Dis. 5, Suppl. 2 (1982) 126–128
Childs, B. and Nyhan, W. L. Further observations of a patient with hyperglycinemia.Pediatrics 33 (1964) 403–412
Childs, B., Nyhan, W. L., Borden, M., Bard, L. and Cooke, R. E. Idiopathic hyperglycinemia: a new disorder of amino acid metabolism.Pediatrics 27 (1961) 522–538
Gerritsen, T., Kaveggia, E. and Waisman, H. A. A. A new type of idiopathic hyperglycinemia with hypo-oxaluria.Pediatrics 36 (1965) 882–891
de Groot, C. J., Troelstra, J. A. and Hommes, F. A. The enzymatic defect of the nonketotic form of hyperglycinemia.Pediatr. Res. 4 (1970) 238–243
Krieger, I. and Nigro, M. Evidence for defective threonine metabolism in non-ketotic hyperglycinaemia.J. Inher. Metab. Dis. 6 (1983) 40–43
Nyhan, W. L., Borden, M. and Childs, B. Idiopathic hyperglycinemia: a new disorder of amino acid metabolism.Pediatrics 27 (1961) 539–550
Palmer, T., Rossiter, M. A., Levin, B. and Oberholzer, V. G. The effect of protein loads on plasma amino acid levels.Clin. Sci. Mol. Med. 45 (1973) 827–832
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Palmer, T., Oberholzer, V.G. Amino acid loading tests in a patient with non-ketotic hyperglycinaemia. J Inherit Metab Dis 8 (Suppl 2), 125–126 (1985). https://doi.org/10.1007/BF01811490
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DOI: https://doi.org/10.1007/BF01811490