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Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease.

Type III glycogen storage disease is caused by a deficiency of glycogen debranching-enzyme activity. Many patients with this disease have both liver and muscle involvement, whereas others have only liver involvement without clinical or laboratory evidence of myopathy. To improve our understanding of...

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Main Authors: Chen, Y T, He, J K, Ding, J H, Brown, B I
格式: Artigo
語言:Inglês
出版: 1987
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684360/
https://ncbi.nlm.nih.gov/pubmed/2961257
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