A fatal case of 2-keto-, 2-hydroxy- and 2-aminoadipic aciduria: Relation of organic aciduria to phenotype?-Reference-Cited by-同舟云学术

A fatal case of 2-keto-, 2-hydroxy- and 2-aminoadipic aciduria: Relation of organic aciduria to phenotype?

Published:1992-03 Issue:2 Volume:15 Page:279-280
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Jakobs C.,de Grauw A. J. C.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF01799643

Reference2 articles.

1. Goodman, S. I. and Frerman, F. E. Organic acidemias due to defects in lysine oxidation. In Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D. (eds.)The Metabolic Basis of Inherited Disease, 6th edn, McGraw-Hill, New York, 1989, pp. 845–855

2. Przyrembel, H. Defects of lysine degradation. In Fernandes, J., Saudubray, J. M. and Tada, K. (eds.)Inborn Metabolic Diseases: Diagnosis and Treatment, Springer-Verlag, Berlin, 1990, pp. 301–311

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