Publikationen von M. Klugmann

El-Kordi, A.; Kästner, A.; Grube, S.; Klugmann, M.; Begemann, M.; Sperling, S.; Hammerschmidt, K.; Hammer, C.; Stepniak, B.; Patzig, J. et al.; Monasterio-Schrader, P. d.; Strenzke, N.; Flügge, G.; Werner, H. B.; Pawlak, R.; Nave, K.-A.; Ehrenreich, H.: A single gene defect causing claustrophobia. Translational Psychiatry 3, e254 (2013)

Al-Saktawi, K.; McLaughlin, M.; Klugmann, M.; Schneider, A.; Barrie, J. A.; McCulloch, M. C.; Montague, P.; Kirkham, D.; Nave, K.-A.; Griffiths, I. R.: Genetic background determines phenotypic severity of the Plp rumpshaker mutation. Journal of Neuroscience Research 72 (1), S. 12 - 24 (2003)

Garbern, J. Y.; Yool, D. A.; Moore, G. J.; Wilds, I. B.; Faulk, M. W.; Klugmann, M.; Nave, K.-A.; Sistermans, E. A.; van der Knaap, M. S.; Bird, T. D. et al.; Shy, M. E.; Kamholz, J. A.; Griffiths, I. R.: Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation. Brain 125 (3), S. 551 - 561 (2002)

Yool, D.; Klugmann, M.; Barrie, J. A.; McCulloch, M. C.; Nave, K.-A.; Griffiths, I. R.: Observations on the structure of myelin lacking the major proteolipid protein. Neuropathology and Applied Neurobiology 28 (1), S. 75 - 78 (2002)