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PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies
Pareyson, D., Botti, S., Sghirlanzoni, A., Taroni, F.Volume:
49
Language:
english
Journal:
Neurology
DOI:
10.1212/WNL.49.5.1478
Date:
November, 1997
File:
PDF, 220 KB
english, 1997