Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0601_151.pdf
Reference28 articles.
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3. Mathews, K.D., et al. Phenotypic and pathological evaluation of the myd mouse, a candidate model for facioscapulohumeral dystrophy. J. Neuropathol. Exp. Neurol. 54, 601–606 (1995).
4. Mathews, K.D., Mills, K.A., Bailey, H., Schelper, R. & Murray, J. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q. Muscle Nerve S2, S98–S102 (1995).
5. Mills, K.A., et al. Genetic mapping near the myd locus on mouse chromosome 8. Mamm. Genome 6, 278–280 (1995).
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