INHERITED DISORDERS OF 3-METHYLCROTONYL COA CARBOXYLATION

被引：28

作者：

LEONARD, JV

SEAKINS, JWT

BARTLETT, K

HYDE, J

WILSON, J

CLAYTON, B

机构：

[1] INST CHILD HLTH,DEPT CHEM PATHOL,LONDON WC1N 1EH,ENGLAND

[2] HOSP SICK CHILDREN,DEPT NEUROL,LONDON WC1N 3JH,ENGLAND

[3] ROYAL VICTORIA INFIRM,DEPT CLIN BIOCHEM,NEWCASTLE TYNE NE1 4LP,TYNE & WEAR,ENGLAND

来源：

ARCHIVES OF DISEASE IN CHILDHOOD | 1981年 / 56卷 / 01期

关键词：

D O I：

10.1136/adc.56.1.53

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：53 / 59

页数：7

共 23 条

[11] EVIDENCE FOR ENZYMIC DEFECT IN BETA-METHYLCROTONYLGLYCINURIA [J].

GOMPERTZ, D ;

GOODEY, PA ;

BARTLETT, K .

FEBS LETTERS, 1973, 32 (01) :13-14

[12] ORGANIC ACIDURIA [J].

KEETON, BR ;

MOOSA, A .

ARCHIVES OF DISEASE IN CHILDHOOD, 1976, 51 (08) :636-638

[13] INCREASED URINARY-EXCRETION OF 3-HYDROXYISOVALERIC ACID IN PATIENTS WITH KETOACIDOSIS [J].

LANDAAS, S .

CLINICA CHIMICA ACTA, 1974, 54 (01) :39-46

[14] CASE OF BIOTIN-RESPONSIVE 3-METHYLCROTONYLGLYCIN AND 3-HYDROXYISOVALERIC ACIDURIA [J].

LEHNERT, W ;

NIEDERHOFF, H ;

JUNKER, A ;

SAULE, H ;

FRASCH, W .

EUROPEAN JOURNAL OF PEDIATRICS, 1979, 132 (02) :107-114

[15]

LEONARD JV, 1979, LANCET, V1, P680

[16]

LEVY HL, 1973, PEDIATRICS, V52, P83

[17]

LOWRY OH, 1951, J BIOL CHEM, V193, P265

[18]

MUNNICH A, 1980, LANCET, V1, P1080

[19]

RASMUSSEN K, J INHERITED METABOL

[20]

Robinson F. A., 1966, VITAMIN COFACTORS EN

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