Publication Date:
2012
Short description:
Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia / Zimoń, M., Baets, J., Almeida-Souza, L., De Vriendt, E., Nikodinovic, J., Parman, Y., Battalo Gcaron Lu, E., Matur, Z., Guergueltcheva, V., Tournev, I., Auer-Grumbach, M., De Rijk, P., Petersen, B.s., Müller, T., Fransen, E., Van Damme, P., Löscher, W.n., Barišić, N., Mitrovic, Z., Previtali, S., et al.. - In: NATURE GENETICS. - ISSN 1061-4036. - 44:10(2012), pp. 1080-1083. [10.1038/ng.2406]
Iris type:
1.1 Articolo in rivista
List of contributors:
Zimoń, M; Baets, J; Almeida-Souza, L; De Vriendt, E; Nikodinovic, J; Parman, Y; Battalo Gcaron Lu, E; Matur, Z; Guergueltcheva, V; Tournev, I; Auer-Grumbach, M; De Rijk, P; Petersen, Bs; Müller, T; Fransen, E; Van Damme, P; Löscher, Wn; Barišić, N; Mitrovic, Z; Previtali, S; Topalo Gcaron Lu, H; Bernert, G; Beleza-Meireles, A; Todorovic, S; Savic-Pavicevic, D; Ishpekova, B; Lechner, S; Peeters, K; Ooms, T; Hahn, Af; Züchner, S; Timmerman, V; Van Dijck, P; Rasic, Vm; Janecke, Ar; De Jonghe, P; Jordanova, A.
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