CARRIER DETECTION FOR SANFILIPPO-A SYNDROME

被引：10

作者：

MATALON, R ^{[1
]}

DEANCHING, M ^{[1
]}

MARBACK, R ^{[1
]}

MICHALS, K ^{[1
]}

机构：

[1] UNIV ILLINOIS, DEPT NUTR, CHICAGO, IL 60612 USA

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1988年 / 11卷 / 02期

关键词：

D O I：

10.1007/BF01799865

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：158 / 160

页数：3

共 10 条

[1]

HALL CW, 1978, METHOD ENZYMOL, V50, P447

[2] MUCOPOLYSACCHARIDOSIS III A (SANFILIPPO A DISEASE) - DEFICIENCY OF A HEPARIN SULFAMIDASE IN SKIN FIBROBLASTS AND LEUKOCYTES [J].

KRESSE, H .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1973, 54 (03) :1111-1118

[3]

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

[4]

MATALON R, 1980, PEDIATR RES, V14, P524

[5] SANFILIPPO A SYNDROME - SULFAMIDASE DEFICIENCY IN CULTURED SKIN FIBROBLASTS AND LIVER [J].

MATALON, R ;

DORFMAN, A .

JOURNAL OF CLINICAL INVESTIGATION, 1974, 54 (04) :907-912

[6] HURLERS SYNDROME - BIOSYNTHESIS OF ACID MUCOPOLYSACCHARIDES IN TISSUE CULTURE [J].

MATALON, R ;

DORFMAN, A .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1966, 56 (04) :1310-&

[7]

MATALON R, 1973, PEDIATR RES, V7, pA384

[8]

ROBBIN DL, 1983, MUSCULOSKELETAL DISE, P381

[9]

VANDEKAMP JJP, 1981, CLIN GENET, V20, P152

[10] LABORATORY DIAGNOSIS OF SANFILIPPO DISEASE [J].

WHITEMAN, P ;

YOUNG, E .

CLINICA CHIMICA ACTA, 1977, 76 (01) :139-147

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