Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleDe novo mutation of the myelin Po gene in Déjérine-Sottas disease (hereditary motor and sensory neuropathy type III): Two amino acid insertion after Asp 118.AuthorsIkegami, Tohru; Nicholson, Garth; Ikeda, Hiroyuki; Ishida, Akihiro; Johnston, Heather; Wise, Grahame; Ouvrier, Robert; Hayasaka, KiyoshiPublicationHuman Mutation, 1998, Vol 11, pS103ISSN1059-7794Publication typeArticleDOI10.1002/humu.1380110134