Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease

D. Pareyson*, D. Menichella, S. Botti, A. Sghirlanzoni, E. Fallica, M. Mora, C. Ciano, M. E. Shy, F. Taroni

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations
Original languageEnglish (US)
Pages (from-to)477-480
Number of pages4
JournalAnnals of the New York Academy of Sciences
Volume883
DOIs
StatePublished - Jan 1 1999

ASJC Scopus subject areas

  • Neuroscience(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • History and Philosophy of Science

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