Relationship between the two immunologically distinguishable forms of glucocerebrosidase in tissue extracts
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1987.tb10907.x/fullpdf
Reference32 articles.
1. Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's disease
2. A Deficiency of Glucocerebrosidase in Gaucher's Disease
3. Deficient activity of glucocerebrosidase in urine from patients with type 1 Gaucher disease
4. 4. R. O. Brady, J. A. Barranger, J. B. Stanbury, J. B. Wijngaarden, D. S. Frederickson, J. L. Goldstein, and M. S. Brown (1983 ) inThe metabolic basis of inherited diseases () pp.842 -856 , McGraw-Hill, New York.
5. Enzyme replacement therapy in Gaucher's disease: large-scale purification of glucocerebrosidase suitable for human administration.
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