BENIGN CLINICAL PRESENTATION OF 3-METHYLCROTONYLGLYCINURIA

被引:11
作者
PEARSON, MA
ALECK, KA
HEIDENREICH, RA
机构
[1] UNIV ARIZONA,COLL MED,STEELE MEM CHILDRENS RES CTR,DEPT PEDIAT,MED & MOLEC GENET SECT,TUCSON,AZ 85724
[2] MARICOPA MED CTR,DEPT PEDIATR,PHOENIX,AZ
关键词
D O I
10.1007/BF02436012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:640 / 641
页数:2
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    BARASH, V
    JAKOBS, C
    GLICK, B
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