Dicarboxylic aminoaciduria.
作者信息
Kamoun P, Parvy P, Rabier D, Bardet J, Billette de Villemeur T, Saudubray J M
机构信息
Laboratoire de Biochimie médicale B, Hôpital Necker-Enfants Malades, Paris, France.
出版信息
J Inherit Metab Dis. 1994;17(6):758. doi: 10.1007/BF00712024.
PMID:7707705
Abstract
摘要
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本文引用的文献
1
Dicarboxylic aminoaciduria: an inborn error of glutamate and aspartate transport with metabolic implications, in combination with a hyperprolinemia.二羧酸氨基酸尿症：一种谷氨酸和天冬氨酸转运的先天性缺陷，伴有代谢影响，并与高脯氨酸血症相关。
Metabolism. 1974 Feb;23(2):115-23. doi: 10.1016/0026-0495(74)90108-5.
2
Dicarboxylic aminoaciduria: an inborn error of amino acid conservation.二羧酸氨基酸尿症：一种氨基酸代谢先天性缺陷病。
J Pediatr. 1977 Sep;91(3):422-7. doi: 10.1016/s0022-3476(77)81312-7.
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