Author:
Argov Zohar,Mitrani-Rosenbaum Stella
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Neurology (clinical),Pharmacology
Reference31 articles.
1. 3rd ser.;Z Argov,2007
2. Eisenberg I, Avidan N, Potikha T, et al. The UDP-N-Acetylglucosamine 2-epimerase/N-Acetylemannosamine kinase is mutated in recessive hereditary inclusion body myopathy. Nat Genet 2001;29: 83–87.
3. Keppler OT, Hinderlich S, Langner J, Schwartz-Albiez R, Reutter W, Pawlita M. UDP-GlcNAc 2-epimerase: a regulator of cell surface sialylation. Science 1999;284: 1372–1376.
4. Argov Z, Soffer D. Hereditary inclusion body myopathies. In: Karpati G, editor. Structural and molecular basis of skeletal muscle disease. ISN Neuropath Press, Basel, 2002;274–276.
5. Fukuda T, Ewan L, Bauer M, et al. Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease. Ann Neurol 2006;59: 700–708.
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