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
UEA Research Groups:	Faculty of Medicine and Health Sciences > Research Groups > Musculoskeletal Medicine
Depositing User:	EPrints Services
Date Deposited:	25 Nov 2010 11:13
Last Modified:	24 Oct 2022 02:22
URI:	https://ueaeprints.uea.ac.uk/id/eprint/15321
DOI:	10.1038/ng1649

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