G.P.87 Demyelinating neuropathy caused by point mutations in PMP22 gene: Phenotype variability

✍ Scribed by Nascimento, A.; Grazia, S.; Otez, C.; Poo, P.; Polo, A.; Jimenez-Mallebrera, C.; Baas, F.; Galvez, H.; Iturriaga, C.; Colomer, J.

• Book ID: 119333843
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 47 KB
• Volume: 22
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2012.06.217