GC-MS IDENTIFICATION OF URINARY SUCCINYLACETONE IN 2 CASES OF HEREDITARY TYROSINEMIA

被引：4

作者：

DIVRY, P

ROLLAND, MO

TESSIER, J

DESAGE, M

COTTE, J

机构：

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1982年 / 5卷

关键词：

D O I：

10.1007/BF01799819

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：41 / 42

页数：2

共 8 条

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[2]

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[3]

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[4]

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[5] ACUTE HEREDITARY TYROSINEMIA TYPE-I - CLINICAL, BIOCHEMICAL AND HEMATOLOGICAL STUDIES IN TWINS [J].

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PATRICK, AD ;

PRESTON, FE ;

WHITFIELD, MF .

JOURNAL OF INHERITED METABOLIC DISEASE, 1981, 4 (01) :37-40

[6] ENZYMATIC DEFICIENCY IN TYROSINEMIA [J].

LADU, BN .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1967, 113 (01) :54-&

[7] ENZYMIC DEFECTS IN HEREDITARY TYROSINEMIA [J].

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LINDSTEDT, S ;

STEEN, G .

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[8]

ROLLAND MO, 1971, THESIS LYON

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