Stephan Züchner
Center for Human Genetics
Duke University Medical Center
595 LaSalle Street
Box 3445 DUMC
USA
Name/email consistency: high
- Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2. Züchner, S., De Jonghe, P., Jordanova, A., Claeys, K.G., Guergueltcheva, V., Cherninkova, S., Hamilton, S.R., Van Stavern, G., Krajewski, K.M., Stajich, J., Tournev, I., Verhoeven, K., Langerhorst, C.T., de Visser, M., Baas, F., Bird, T., Timmerman, V., Shy, M., Vance, J.M. Ann. Neurol. (2006)
- Molecular genetics of autosomal-dominant axonal Charcot-Marie-Tooth disease. Züchner, S., Vance, J.M. Neuromolecular Med. (2006)
- Emerging pathways for hereditary axonopathies. Züchner, S., Vance, J.M. J. Mol. Med. (2005)