Author:
Poitelon Yannick,Kozlov Serguei,Devaux Jerôme,Vallat Jean-Michel,Jamon Marc,Roubertoux Pierre,Rabarimeriarijaona Sitraka,Baudot Cécile,Hamadouche Tarik,Stewart Colin L.,Levy Nicolas,Delague Valérie
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology,Molecular Medicine
Reference54 articles.
1. Achilli, F., Bros-Facer, V., Williams, H. P., Banks, G. T., AlQatari, M., Chia, R., et al. (2009). An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Disease Models & Mechanisms, 2(7–8), 359–373.
2. Benedetti, S., Bertini, E., Iannaccone, S., Angelini, C., Trisciani, M., Toniolo, D., et al. (2005). Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy. Journal of Neurology, Neurosurgery and Psychiatry, 76(7), 1019–1021.
3. Bouhouche, A., Birouk, N., Azzedine, H., Benomar, A., Durosier, G., Ente, D., et al. (2007). Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): Phenotype-genotype correlations in 13 Moroccan families. Brain, 130(Pt 4), 1062–1075.
4. Brancolini, C., Marzinotto, S., Edomi, P., Agostoni, E., Fiorentini, C., Muller, H. W., et al. (1999). Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22. Molecular Cell Biology, 10(7), 2441–2459.
5. Chaouch, M., Allal, Y., De Sandre-Giovannoli, A., Vallat, J. M., Amer-el-Khedoud, A., Kassouri, N., et al. (2003). The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene. Neuromuscular Disorders, 13(1), 60–67.
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