We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitlePhenotypic spectrum of hereditary neuralgic amyotrophy caused by the SEPT9 R88W mutationAuthorsUeda, M; Kawamura, N; Tateishi, T; Sakae, N; Motomura, K; Ohyagi, Y; Kira, J-iPublicationJournal of Neurology, Neurosurgery & Psychiatry, 2010, Vol 81, Issue 1, p94ISSN0022-3050Publication typearticleDOI10.1136/jnnp.2008.168260