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

Kuhlenbaumer, Gregor, Hannibal, Mark C., Nelis, Eva, Schirmacher, Anja, Verpoorten, Nathalie, Meuleman, Jan, Watts, Giles D. J., De Vriendt, Els, Young, Peter, Stögbauer, Florian, Halfter, Hartmut, Irobi, Joy, Goossens, Dirk, Del-Favero, Jurgen, Betz, Benjamin G., Hor, Hyun, Kurleman, Gert, Bird, Thomas D., Airaksinen, Eila, Mononen, Tarja, Pou Serradell, Adolfo, Prats, José M., Van Broeckhoven, Christine, De Jonghe, Peter, Timmerman, Vincent, Ringelstein, E. Bernd and Chance, Phillip F. (2005) Mutations in the human septin 0 gene (SEPT9) cause hereditary neuralgic amyotrophy (HNA). Nature Genetics, 37 (10). pp. 1044-1046. ISSN 1546-1718

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Item Type: Article
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
Depositing User: EPrints Services
Date Deposited: 25 Nov 2010 11:13
Last Modified: 21 Apr 2020 20:05
URI: https://ueaeprints.uea.ac.uk/id/eprint/15321
DOI: 10.1038/ng1649

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