Tryptophan and lysine metabolism in alpha-aminoadipic aciduria-Reference-Cited by-同舟云学术

Tryptophan and lysine metabolism in alpha-aminoadipic aciduria

Published:1980 Issue:1 Volume:5 Page:35-41
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Fischer Milton H.,Brown Raymond R.

Publisher

Wiley

Subject

Genetics (clinical)

Reference11 articles.

1. α-Amino adipic aciduria in an oligophrenic child

2. : α-Aminoadipic aciduria, a new inborn error of lysine metabolism. In (eds): “Inborn Errors of Calcium and Bone Metabolism,” Lancaster, Great Britain: MTP Press Ltd, 1976, pp 267-270.

3. : Abnormalities of branched-chain amino acid metabolism. In (eds): “The Metabolic Basis of Inherited Disease.” 4th Ed. New York: McGraw-Hill Book Co, 1978, pp 397-410.

4. Alpha-Aminoadipate aminotransferase and kynurenine aminotransferase. Purification, characterization, and further evidence for identity.

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