D. Bönsch
Institut für Klinische Chemie und Laboratoriumsdiagnostik
Klinikum der Universität Jena
Germany
Name/email consistency: high
- Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene. Bönsch, D., Schwindt, A., Navratil, P., Palm, D., Neumann, C., Klimpe, S., Schickel, J., Hazan, J., Weiller, C., Deufel, T., Liepert, J. J. Neurol. Neurosurg. Psychiatr. (2003)
- A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus. Bönsch, D., Scheer, P., Neumann, C., Lang-Roth, R., Seifert, E., Storch, P., Weiller, C., Lamprecht-Dinnesen, A., Deufel, T. Eur. J. Hum. Genet. (2001)