Mechanisms of Disease: congenital muscular dystrophies—glycosylation takes center stage
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical)
Link
http://www.nature.com/articles/ncpneuro0155.pdf
Reference63 articles.
1. Jimenez-Mallebrera C et al. (2005) Congenital muscular dystrophy: molecular and cellular aspects. Cell Mol Life Sci 62: 809–823
2. van Reeuwijk J et al. (2005) Glyc-O-genetics of Walker–Warburg syndrome. Clin Genet 67: 281–289
3. Martin PT and Freeze HH (2003) Glycobiology of neuromuscular disorders. Glycobiology 13: 67R–75R
4. Muntoni F et al. (2002) Defective glycosylation in muscular dystrophy. Lancet 360: 1419–1421
5. Michele DE and Campbell KP (2003) Dystrophin–glycoprotein complex: post-translational processing and dystroglycan function. J Biol Chem 278: 15457–15460
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