CONGENITAL LACTIC-ACIDOSIS, ALPHA-KETOGLUTARIC ACIDURIA AND VARIANT FORM OF MAPLE SYRUP URINE DISEASE DUE TO A SINGLE ENZYME DEFECT - DIHYDROLIPOYL DEHYDROGENASE-DEFICIENCY

被引：35

作者：

MUNNICH, A

SAUDUBRAY, JM

TAYLOR, J

CHARPENTIER, C

MARSAC, C

ROCCHICCIOLI, F

AMEDEEMANESME, O

COUDE, FX

FREZAL, J

ROBINSON, BH

机构：

[1] LAB BIOCHIM,INSERM,U75,PARIS,FRANCE

[2] HOP ENFANTS MALAD,INSERM,U12,UNITE RECH GENET MED,F-75730 PARIS 15,FRANCE

[3] UNIV TORONTO,DEPT BIOCHEM,TORONTO M5S 1A1,ONTARIO,CANADA

[4] HOSP SICK CHILDREN,RES INST,TORONTO M5G 1X8,ONTARIO,CANADA

来源：

ACTA PAEDIATRICA SCANDINAVICA | 1982年 / 71卷 / 01期

关键词：

D O I：

10.1111/j.1651-2227.1982.tb09393.x

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：167 / 171

页数：5

共 12 条

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