ORGANIC ACIDURIA IN NEONATAL MULTIPLE CARBOXYLASE DEFICIENCY

被引：20

作者：

SWEETMAN, L

NYHAN, WL

SAKATI, NA

OHLSSON, A

MANGE, MS

BOYCHUK, RB

KAYE, R

机构：

[1] KING FAISAL SPECIALIST HOSP,DEPT PEDIATR,RIYADH,SAUDI ARABIA

[2] DHAHRAN HLTH CTR,DHAHRAN,SAUDI ARABIA

[3] KAPEOLANI CHILDRENS MED CTR,HONOLULU,HI

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1982年 / 5卷 / 01期

关键词：

D O I：

10.1007/BF01799754

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：49 / 53

页数：5

共 26 条

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[7]

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[8]

ELDJARN L, 1970, LANCET, V2, P521

[9] IDENTIFICATION OF TRIGLYLGLYCINE IN URINE OF A CHILD WITH BETA-METHYLCROTONYLGLYCINURIA [J].

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[10] CHILD WITH A DEFECT IN LEUCINE METABOLISM ASSOCIATED WITH BETA-HYDROXYISOVALERIC ACIDURIA AND BETA-METHYLCROTONYLGLYCINURIA [J].

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