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Inherited neuropathies and deafness caused by a PMP22 point mutation: a case report and a review of the literature

Research output: Contribution to journalArticle

Abstract

No abstract
Original languageEnglish
Pages (from-to)N/A-N/A
JournalNeurological Sciences
Issue numberN/A
DOIs
Publication statusPublished - 2012

Keywords

  • CMT

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