Clinical, biochemical and genetic findings in three patients with a β-ureidopropionase deficiency

被引：0
|
作者：
van Kuilenburg, A. B. P. [1 ]
Meijer, J. [1 ]
Saito, K. [2 ]
Eto, K. [3 ]
Meinsma, R. [1 ]
Abeling, N. G. G. M. [1 ]
Zoetekouw, L. [1 ]
Assmann, B. [4 ]
机构：
[1] AMC, Genet Metab Dis, Clin Chem, Amsterdam, Netherlands
[2] Tokyo Womens Med Univ, Inst Med Genet, Tokyo, Japan
[3] Tokyo Womens Med Univ, Dept Pediat, Tokyo, Japan
[4] Univ Child Hosp, Dept Gen Pediat, Dusseldorf, Germany
来源：
JOURNAL OF INHERITED METABOLIC DISEASE | 2008年 / 31卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
618P
引用
收藏
页码：155 / 155
页数：1
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