Mutations in the human septin 0 gene (SEPT9) cause hereditary neuralgic amyotrophy (HNA)

Gregor Kuhlenbaumer, Mark C. Hannibal, Eva Nelis, Anja Schirmacher, Nathalie Verpoorten, Jan Meuleman, Giles D. J. Watts, Els De Vriendt, Peter Young, Florian Stögbauer, Hartmut Halfter, Joy Irobi, Dirk Goossens, Jurgen Del-Favero, Benjamin G. Betz, Hyun Hor, Gert Kurleman, Thomas D. Bird, Eila Airaksinen, Tarja MononenAdolfo Pou Serradell, José M. Prats, Christine Van Broeckhoven, Peter De Jonghe, Vincent Timmerman, E. Bernd Ringelstein, Phillip F. Chance

Research output: Contribution to journalArticle

173 Citations (Scopus)
Original languageEnglish
Pages (from-to)1044-1046
Number of pages3
JournalNature Genetics
Volume37
Issue number10
DOIs
Publication statusPublished - 2005

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