一名患有α-酮己二酸和α-氨基己二酸尿症的患者。 - Suppr

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A patient with alpha-ketoadipic and alpha-aminoadipic aciduria.

作者信息

Duran M, Beemer F A, Wadman S K, Wendel U, Janssen B

出版信息

J Inherit Metab Dis. 1984;7(2):61. doi: 10.1007/BF01805803.

DOI:10.1007/BF01805803

PMID:6434826

Abstract

摘要

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本文引用的文献

Tryptophan and lysine metabolism in alpha-aminoadipic aciduria.

Am J Med Genet. 1980;5(1):35-41. doi: 10.1002/ajmg.1320050106.

Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studies.α-酮己二酸尿症，一种新的赖氨酸代谢先天性缺陷；生化研究

Clin Chim Acta. 1975 Feb 8;58(3):257-69. doi: 10.1016/0009-8981(75)90445-3.

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