MAROTEAUX-LAMY DISEASE (MUCOPOLYSACCHARIDOSIS-VI) SUBTYPE-A - DEFICIENCY OF A N-ACETYLGALACTOSAMINE-4-SULFATASE

被引：81

作者：

OBRIEN, JF ^{[1
]}

CANTZ, M ^{[1
]}

SPRANGER, J ^{[1
]}

机构：

[1] UNIV KIEL,DEPT PEDIAT,D-23 KIEL,WEST GERMANY

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 1974年 / 60卷 / 03期

关键词：

D O I：

10.1016/0006-291X(74)90435-5

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：1170 / 1177

页数：8

共 21 条

[1] DEFECT IN HUNTER SYNDROME - DEFICIENCY OF SULFOIDURONATE SULFATASE [J].

BACH, G ;

EISENBERG, F ;

CANTZ, M ;

NEUFELD, EF .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (07) :2134-2138

[2] DEFECT IN HURLER AND SCHEIE SYNDROMES - DEFICIENCY OF ALPHA-IDURONIDASE [J].

BACH, G ;

WEISSMAN.B ;

FRIEDMAN, R ;

NEUFELD, EF .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (08) :2048-&

[3] DISTINCT BIOCHEMICAL DEFICIT IN MAROTEAUX-LAMY SYNDROME (MUCOPOLYSACCHARIDOSIS VI) [J].

BARTON, RW ;

NEUFELD, EF .

JOURNAL OF PEDIATRICS, 1972, 80 (01) :114-+

[4] THE ASSAY OF ARYLSULPHATASE-A AND ARYLSULPHATASE-B IN HUMAN URINE [J].

BAUM, H ;

DODGSON, KS ;

SPENCER, B .

CLINICA CHIMICA ACTA, 1959, 4 (03) :453-455

[5]

CANTZ M, 1972, METHOD ENZYMOL, V28, P884

[6]

CANTZ M, BIRTH DEFECTS OAS

[7]

CANTZ M, IN PRESS

[8]

DIFERRANTE N, 1974, HOPKINS MED J, V135, P42

[9]

GEHLER J, 1974, HUMANGENETIK, V23, P149

[10]

MAROTEAUX B, 1969, PRESSE MED, V71, P1849

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