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G.P.87 Demyelinating neuropathy caused by point mutations in PMP22 gene: Phenotype variability
Nascimento, A., Grazia, S., Otez, C., Poo, P., Polo, A., Jimenez-Mallebrera, C., Baas, F., Galvez, H., Iturriaga, C., Colomer, J.Volume:
22
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2012.06.217
Date:
October, 2012
File:
PDF, 47 KB
english, 2012