Author:
Sweetman L.,Nyhan W. L.,Cravens J.,Zomer Y.,Plunket D. C.
Subject
Genetics (clinical),Genetics
Reference21 articles.
1. Ando, T., Klingberg, W. G., Ward, A. N., Rasmussen, K. and Nyhan, W. L. Isovaleric acidemia presenting with altered metabolism of glycine.Pediatr. Res. 5 (1971) 478–486
2. Ando, T., Nyhan, W. L., Bachmann, C., Rasmussen, K., Scott, R. and Smith, E. K. Isovaleric acidemia: Identification of isovalerate, isovalerylglycine, and 3-hydroxyisovalerate in urine of a patient previously reported as having butyric and hexanoic acidemia.J. Pediatr. 82 (1973) 243–248
3. Ando, T. and Nyhan, W. L. Propionic acidemia and ketotic hyperglycinemia syndrome. In Nyhan, W. L. (ed.)Heritable Disorders of Amino Acid Metabolism J. Wiley, New York, 1974, pp. 37–60
4. Barnes, N. D., Hull, D., Balgobin, L. and Gompertz, D. Biotin responsive propionic acidemia.Lancet 2 (1970) 244–245
5. Brandt, I. K., Hsia, Y. E., Clement, D. H. and Provence, S. A. Propionicacidemia (ketotic hyperglycinemia): Dietary treatment resulting in normal growth and development.Pediatrics 53 (1974) 391–395
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