Several forms of muscular dystrophy are associated with mutations in genes that regulate glycosylation of α-dystroglycan. Forced overexpression of one of these genes, LARGE, in mice overcomes the defective glycosylation present in this group of disorders (pages 696–703).
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References
Laval, S.H. & Bushby, K.M. Neuropathol. Appl. Neurobiol. 30, 91–105 (2004).
Muntoni, F., Brockington, M., Torelli, S. & Brown, S.C. Curr. Opin. Neurol. 17, 205–209 (2004).
Winder, S.J. Trends Biochem. Sci. 26, 118–124 (2001).
Michele, D.E. & Campbell, K.P. J. Biol. Chem. 278, 15457–15460 (2003).
Barresi, R. et al. Nat. Med. 10, 696–703 (2004).
Michele, D.E. et al. Nature 418, 417–422 (2002).
Longman, C. et al. Hum. Mol. Genet. 12, 2853–2861 (2003).
Grewal, P.K., Holzfeind, P.J., Bittner, R.E. & Hewitt, J.E. Nat. Genet. 28, 151–154 (2001).
Henry, M.D. & Campbell, K.P. Curr. Opin. Cell. Biol. 11, 602–607 (1999).
Endo, T. Biochim. Biophys. Acta 1473, 237–246 (1999).
Kim, D.S. et al. Neurology 62, 1009–1011 (2004).
Talts, J.F., Andac, Z., Gohring, W., Brancaccio, A. & Timpl, R. EMBO J. 18, 863–870 (1999).
Kanagawa, M. et al. Cell published online 3 June 2004 (doi: 10.1016/5009286704005434).
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Muntoni, F., Brockington, M. & Brown, S. Glycosylation eases muscular dystrophy. Nat Med 10, 676–677 (2004). https://doi.org/10.1038/nm0704-676
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DOI: https://doi.org/10.1038/nm0704-676