POSTTRANSLATIONAL PROCESSING OF HUMAN LYSOSOMAL ACID BETA-GLUCOSIDASE - A CONTINUUM OF DEFECTS IN GAUCHER DISEASE TYPE-1 AND TYPE-2 FIBROBLASTS

被引：0

作者：

BERGMANN, JE ^{[1
]}

GRABOWSKI, GA ^{[1
]}

机构：

[1] CUNY MT SINAI SCH MED,DIV MED & MOLEC GENET,DEPT PEDIAT,NEW YORK,NY 10029

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1989年 / 44卷 / 05期

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：741 / 750

页数：10

共 50 条

[1] GAUCHER DISEASE - INSITU MOLECULAR-SIZE OF MEMBRANE-BOUND ACID BETA-GLUCOSIDASE IN TYPE-1, TYPE-2 AND TYPE-3 GAUCHER FIBROBLASTS
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[7] SUCROSE GRADIENT ANALYSIS OF PHOSPHOLIPID-ACTIVATED BETA-GLUCOSIDASE IN TYPE-1 AND TYPE-2 GAUCHERS-DISEASE
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[8] Enzyme therapy in Gaucher disease type 1: Effect of neutralizing antibodies to acid beta-glucosidase
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[10] GAUCHER DISEASE TYPE-1 - CLONING AND CHARACTERIZATION OF A CDNA-ENCODING ACID BETA-GLUCOSIDASE FROM AN ASHKENAZI JEWISH PATIENT
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