Author:
Drost Maarten R.,Schaart Gert,van Dijk Paul,van Capelle Carine I.,van Der Vusse Ger J.,Delhaas Tammo,van Der Ploeg Ans T.,Reuser Arnold J. J.
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Reference12 articles.
1. , . Acid maltase deficiency. In: , editors. Myology, basic and clinical. New York: McGraw-Hill; 2004. p 1559–1586.
2. Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease
3. Autophagy and Lysosomes in Pompe Disease
4. . Glycogen storage disease type II; acid alpha-glucosidase (acid maltase) deficiency. In: , , editors. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill; 2001. p 3389–3420.
5. Recombinant human acid -glucosidase: Major clinical benefits in infantile-onset Pompe disease
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