Author:
Fraites Thomas J.,Schleissing Mary R.,Shanely R.Andrew,Walter Glenn A.,Cloutier Denise A.,Zolotukhin Irene,Pauly Daniel F.,Raben Nina,Plotz Paul H.,Powers Scott K.,Kessler Paul D.,Byrne Barry J.
Subject
Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine
Reference52 articles.
1. An electron microscopic and biochemical study of type II glycogenosis;Baudhin;Lab. Invest.,1964
2. Hirschhorn, R., and Reuser, A. J. J.2000. Glycogen storage disease II: acid-α glucosidase (acid maltase) deficiency. In The Metabolic and Molecular Bases of Inherited DiseaseC. Scriveret al., Eds., pp. 3389–3420. Mc-Graw Hill, New York.
3. α-glucosidase deficiency in generalized glycogen storage disease (Pompe's disease);Hers;Biochem. J.,1963
4. Glycogenosis type II (acid maltase deficiency);Reuser;Muscle Nerve,1995
5. Respiratory insufficiency in adult-type acid maltase deficiency;Moufarrej;South. Med. J.,1993
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