SANFILIPPO SYNDROME - PROFOUND DEFICIENCY OF ALPHA-ACETYLGLUCOSAMINIDASE ACTIVITY IN ORGANS AND SKIN FIBROBLASTS FROM TYPE-B PATIENTS

被引：160

作者：

OBRIEN, JS

机构：

来源：

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | 1972年 / 69卷 / 07期

关键词：

D O I：

10.1073/pnas.69.7.1720

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

引用

页码：1720 / &

共 11 条

[1]

DODION J., 1966, PATHOL EUR, V1, P50

[2]

DORFMAN A, 1972, METABOLIC BASIS INHE, pCH49

[3]

HO MW, 1972, AM J HUM GENET, V24, P37

[4]

KRESSE H, 1972, J BIOL CHEM, V247, P2164

[5] BIOCHEMICAL HETEROGENEITY OF SANFILIPPO SYNDROME - PRELIMINARY CHARACTERIZATION OF 2 DEFICIENT FACTORS [J].

KRESSE, H ;

WIESMANN, U ;

CANTZ, M ;

HALL, CW ;

NEUFELD, EF .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1971, 42 (05) :892-&

[6]

LEROY JM, IN PRESS

[7]

MCKUSICK VA, 1966, HERITABLE DISORDERS, P357

[8] TAY-SACHS DISEASE - PRENATAL DIAGNOSIS [J].

OBRIEN, JS ;

OKADA, S ;

FILLERUP, DL ;

VEATH, ML ;

ADORNATO, B ;

BRENNER, PH ;

LEROY, JG .

SCIENCE, 1971, 172 (3978) :61-&

[9]

OKADA S, 1971, AM J HUM GENET, V23, P55

[10]

ROSEMAN S, 1951, J BIOL CHEM, V191, P607

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