Amylo-1, 6-glucosidase in human fibroblasts: Studies in Type III glycogen storage disease-Reference-Cited by-同舟云学术

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Amylo-1, 6-glucosidase in human fibroblasts: Studies in Type III glycogen storage disease

Published:1970-05 Issue:3 Volume:39 Page:301-306
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Justice Parvin,Ryan Catherine,Hsia David Yi-Yung,Krmpotik Eva

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference12 articles.

1. Enzymatic Debranching of Glycogen: A New Pathway in Rabbit Muscle for the Enzymatic Debranching of Glycogen

2. Culture of Strain L Cells in Suspension: Replacement of Polymer by Traces of Trypsin in A Defined Medium

3. AMYLO-1, 6-GLUCOSIDASE IN MUSCLE TISSUE IN GENERALIZED GLYCOGEN STORAGE DISEASE

4. Structure of Glycogens and Amylopectins

Cited by 23 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Glycogenosis type III/amylo-1,6-glucosidase (debrancher) deficiency;Atlas of Inherited Metabolic Diseases 3E;2011-12-30

2. Radiometric Methods of Enzyme Assay;Methods of Biochemical Analysis;2006-10-31

3. Biochemical diagnosis of hepatic glycogen storage diseases: 20 years French experience;Clinical Biochemistry;1991-04

4. Skin biopsy findings in glycogenosis III: Clinical, biochemical, and electrophysiological correlations;Annals of Neurology;1990-05

5. Debranching enzyme in fibroblasts, amniotic fluid cells and chorionic villi: pre- and postnatal diagnosis of glycogenosis type III;Clinica Chimica Acta;1985-07

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