GALACTOSYLGALACTOSYLGLUCOSYLCERAMIDE - GALACTOSYL HYDROLASE IN NORMAL HUMAN PLASMA AND ITS ABSENCE IN PATIENTS WITH FABRYS DISEASE

被引：42

作者：

MAPES, CA

ANDERSON, RL

SWEELEY, CC

机构：

来源：

关键词：

D O I：

10.1016/0014-5793(70)80151-X

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：180 / &

共 12 条

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[7] HURLERS SYNDROME - DEFICIENCY OF A SPECIFIC BETA GALACTOSIDASE ISOENZYME
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[8] MIYATAKE T, 1969, JPN J EXP MED, V39, P35
[9] TAY-SACHS DISEASE - GENERALIZED ABSENCE OF A BETA-D-N-ACEYLHEXOSAMINIDASE COMPONENT
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[J]. SCIENCE, 1969, 165 (3894) : 698 - &
[10] SWEELEY CC, 1963, J BIOL CHEM, V238, P3148