ABSENCE OF HEPATIC MOLYBDENUM COFACTOR - AN INBORN ERROR OF METABOLISM LEADING TO A COMBINED DEFICIENCY OF SULFITE OXIDASE AND XANTHINE DEHYDROGENASE

被引：53

作者：

WADMAN, SK

DURAN, M

BEEMER, FA

CATS, BP

JOHNSON, JL

RAJAGOPALAN, KV

SAUDUBRAY, JM

OGIER, H

CHARPENTIER, C

BERGER, R

SMIT, GPA

WILSON, J

KRYWAWYCH, S

机构：

[1] DUKE UNIV,MED CTR,DEPT BIOCHEM,DURHAM,NC 27710

[2] HOP ENFANTS MALAD,F-75130 PARIS 15,FRANCE

[3] HOP BICETRE,BIOCHIM LAB,F-94270 KREMLIN BICETRE,FRANCE

[4] UNIV GRONINGEN,DEPT PEDIAT,9712 KZ GRONINGEN,NETHERLANDS

[5] HOSP SICK CHILDREN,LONDON WC1N 3JH,ENGLAND

[6] UNIV COLL HOSP LONDON,SCH MED,RAYNE INST,LONDON WC1E 6JJ,ENGLAND

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1983年 / 6卷

关键词：

D O I：

10.1007/BF01811328

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：78 / 83

页数：6

共 12 条

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[9] INBORN-ERRORS OF MOLYBDENUM METABOLISM - COMBINED DEFICIENCIES OF SULFITE OXIDASE AND XANTHINE DEHYDROGENASE IN A PATIENT LACKING THE MOLYBDENUM COFACTOR [J].

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[10] SULFITE OXIDASE DEFICIENCY - BIOCHEMICAL AND CLINICAL INVESTIGATIONS OF A HEREDITARY METABOLIC DISORDER IN SULFUR METABOLISM [J].

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