Recombinant human α-glucosidase from rabbit milk in Pompe patients
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference4 articles.
1. Glycogen storage disease type II: acid α‐glucosidase (acid maltase) deficiency;Hirschhorn,1995
2. Isolation and characterisation of a recombinant precursor form of lysosomal acid α‐glucosidase;Fuller;Eur J Biochem,1995
3. High level production of recombinant human lysosomal acid α‐glucosidase in Chinese hamster ovary cells which targets to heart muscle and corrects glycogen accumulation in fibroblasts from patients with Pompe disease;Van Hove;Proc Natl Acad Sci USA,1996
4. Human acid α‐glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II;Bijvoet;Hum Molec Genet,1999
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