PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies.

D. Pareyson, S. Botti, A. Sghirlanzoni, F. Taroni

Research output: Contribution to journalArticle

5 Citations (Scopus)
Original languageEnglish
Pages (from-to)1478-1479
Number of pages2
JournalNeurology
Volume49
Issue number5
Publication statusPublished - Nov 1997

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies. / Pareyson, D.; Botti, S.; Sghirlanzoni, A.; Taroni, F.

In: Neurology, Vol. 49, No. 5, 11.1997, p. 1478-1479.

Research output: Contribution to journalArticle

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