Targeted Disruption of the Acid α-Glucosidase Gene in Mice Causes an Illness with Critical Features of Both Infantile and Adult Human Glycogen Storage Disease Type II-Reference-Cited by-同舟云学术

Targeted Disruption of the Acid α-Glucosidase Gene in Mice Causes an Illness with Critical Features of Both Infantile and Adult Human Glycogen Storage Disease Type II

Published:1998-07 Issue:30 Volume:273 Page:19086-19092
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Raben Nina,Nagaraju Kanneboyina,Lee Eunice,Kessler Paul,Byrne Barry,Lee Laura,LaMarca Mary,King Christina,Ward Jerrold,Sauer Brian,Plotz Paul

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference23 articles.

1. Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe disease

2. The Metabolic and Molecular Basis of Inherited Disease;Hirschhorn,1995

3. Receptor-Mediated Uptake of Acid α-Glucosidase Corrects Lysosomal Glycogen Storage in Cultured Skeletal Muscle

4. Intravenous administration of phosphorylated acid alpha-glucosidase leads to uptake of enzyme in heart and skeletal muscle of mice.

5. LYSOSOMAL STORAGE DISEASES

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