Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations

2003

De Sandre-Giovannoli, A., Chaouch, M., Boccaccio, I., Bernard, R., Delague, V., Grid, D., Vallat, J.M., Levy, N. and Megarbane, A.:

J Med Genet 40 (2003) e87.

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