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

2003

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

Journal Of Medical Genetics 40 (2003).