Effect of GNE Mutations on Cytoskeletal Network Proteins: Potential Gateway to Understand Pathomechanism of GNEM
Author:
Funder
bhabha atomic research centre
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology,Molecular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12017-022-08711-4.pdf
Reference56 articles.
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2. Argov, Z. (2015). GNE myopathy: A personal trip from bedside observation to therapeutic trials. Acta Myologica, 33(2), 107–110.
3. Argov, Z., Bronstein, F., Esposito, A., Feinsod-Meiri, Y., Florence, J. M., Fowler, E., Greenberg, M. B., Malkus, E. C., Rebibo, O., Siener, C. S., Caraco, Y., Kolodny, E. H., Lau, H. A., Pestronk, A., Shieh, P., Skrinar, A. M., & Mayhew, J. E. (2017). Characterization of strength and function in ambulatory adults with GNE myopathy. Journal of Clinical Neuromuscular Disease, 19(1), 19–26. https://doi.org/10.1097/CND.0000000000000181
4. Bhattacharya, S., Khadilkar, S. V., Nalini, A., Ganapathy, A., Mannan, A. U., Majumder, P. P., & Bhattacharya, A. (2018). Mutation spectrum of GNE myopathy in the Indian sub-continent. Journal of Neuromuscular Diseases, 5(1), 85–92. https://doi.org/10.3233/JND-170270
5. Bravo-Cordero, J. J., Magalhaes, M. A. O., Eddy, R. J., Hodgson, L., & Condeelis, J. (2013). Functions of cofilin in cell locomotion and invasion. Nature Reviews Molecular Cell Biology, 14, 405–417. https://doi.org/10.1038/nrm3609
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