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 Mononen; Adolfo Pou Serradell; José M. Prats; Christine Van Broeckhoven; Peter De Jonghe; Vincent Timmerman; E. Bernd Ringelstein; Phillip F. Chance

doi:10.1038/ng1649

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

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205 Citations (Scopus)

Original language	English
Pages (from-to)	1044-1046
Number of pages	3
Journal	Nature Genetics
Volume	37
Issue number	10
DOIs	https://doi.org/10.1038/ng1649
Publication status	Published - 2005

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Kuhlenbaumer, G., Hannibal, M. C., Nelis, E., Schirmacher, A., Verpoorten, N., Meuleman, J., Watts, G. D. J., De Vriendt, E., Young, P., Stögbauer, F., Halfter, H., Irobi, J., Goossens, D., Del-Favero, J., Betz, B. G., Hor, H., Kurleman, G., Bird, T. D., Airaksinen, E., ... Chance, P. F. (2005). Mutations in the human septin 0 gene (SEPT9) cause hereditary neuralgic amyotrophy (HNA). Nature Genetics, 37(10), 1044-1046. https://doi.org/10.1038/ng1649

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title = "Mutations in the human septin 0 gene (SEPT9) cause hereditary neuralgic amyotrophy (HNA)",

author = "Gregor Kuhlenbaumer and Hannibal, {Mark C.} and Eva Nelis and Anja Schirmacher and Nathalie Verpoorten and Jan Meuleman and Watts, {Giles D. J.} and {De Vriendt}, Els and Peter Young and Florian St{\"o}gbauer and Hartmut Halfter and Joy Irobi and Dirk Goossens and Jurgen Del-Favero and Betz, {Benjamin G.} and Hyun Hor and Gert Kurleman and Bird, {Thomas D.} and Eila Airaksinen and Tarja Mononen and {Pou Serradell}, Adolfo and Prats, {Jos{\'e} M.} and {Van Broeckhoven}, Christine and {De Jonghe}, Peter and Vincent Timmerman and Ringelstein, {E. Bernd} and Chance, {Phillip F.}",

year = "2005",

doi = "10.1038/ng1649",

language = "English",

volume = "37",

pages = "1044--1046",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Publishing Group",

number = "10",

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Kuhlenbaumer, G, Hannibal, MC, Nelis, E, Schirmacher, A, Verpoorten, N, Meuleman, J, Watts, GDJ, De Vriendt, E, Young, P, Stögbauer, F, Halfter, H, Irobi, J, Goossens, D, Del-Favero, J, Betz, BG, Hor, H, Kurleman, G, Bird, TD, Airaksinen, E, Mononen, T, Pou Serradell, A, Prats, JM, Van Broeckhoven, C, De Jonghe, P, Timmerman, V, Ringelstein, EB & Chance, PF 2005, 'Mutations in the human septin 0 gene (SEPT9) cause hereditary neuralgic amyotrophy (HNA)', Nature Genetics, vol. 37, no. 10, pp. 1044-1046. https://doi.org/10.1038/ng1649

TY - JOUR

T1 - Mutations in the human septin 0 gene (SEPT9) cause hereditary neuralgic amyotrophy (HNA)

AU - Kuhlenbaumer, Gregor

AU - Hannibal, Mark C.

AU - Nelis, Eva

AU - Schirmacher, Anja

AU - Verpoorten, Nathalie

AU - Meuleman, Jan

AU - Watts, Giles D. J.

AU - De Vriendt, Els

AU - Young, Peter

AU - Stögbauer, Florian

AU - Halfter, Hartmut

AU - Irobi, Joy

AU - Goossens, Dirk

AU - Del-Favero, Jurgen

AU - Betz, Benjamin G.

AU - Hor, Hyun

AU - Kurleman, Gert

AU - Bird, Thomas D.

AU - Airaksinen, Eila

AU - Mononen, Tarja

AU - Pou Serradell, Adolfo

AU - Prats, José M.

AU - Van Broeckhoven, Christine

AU - De Jonghe, Peter

AU - Timmerman, Vincent

AU - Ringelstein, E. Bernd

AU - Chance, Phillip F.

PY - 2005

Y1 - 2005

U2 - 10.1038/ng1649

DO - 10.1038/ng1649

M3 - Article

VL - 37

SP - 1044

EP - 1046

JO - Nature Genetics

JF - Nature Genetics

SN - 1061-4036

IS - 10

ER -