Uptake and stability of human and bovine acid α-glucosidase in cultured fibroblasts and skeletal muscle cells from glycogenosis type II patients-Reference-Cited by-同舟云学术

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Uptake and stability of human and bovine acid α-glucosidase in cultured fibroblasts and skeletal muscle cells from glycogenosis type II patients

Published:1984-11 Issue:1 Volume:155 Page:178-189
ISSN:0014-4827
Container-title:Experimental Cell Research
language:en
Short-container-title:Experimental Cell Research

Author:

Reuser A.J.J.,Kroos M.A.,Ponne N.J.,Wolterman R.A.,Loonen M.C.B.,Busch H.F.M.,Visser W.J.,Bolhuis P.A.

Publisher

Elsevier BV

Subject

Cell Biology

Reference41 articles.

1. α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)

2. Lysosomes and storage diseases;Hers,1973

3. The metabolic basis of inherited disease;Howell,1983

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