Inken Körber

The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome.

K. Willecke, T. Moser, N. Strenzke, 2011, Human molecular genetics.

Abnormal microglial activation in the Cstb−/− mouse, a model for progressive myoclonus epilepsy, EPM1

T. Joensuu, A. Lehesjoki, L. Tian, 2015, Glia.

Brain inflammation is accompanied by peripheral inflammation in Cstb−/− mice, a model for progressive myoclonus epilepsy

T. Joensuu, A. Lehesjoki, L. Tian, 2016, Journal of Neuroinflammation.

Gene-Expression Profiling Suggests Impaired Signaling via the Interferon Pathway in Cstb-/- Microglia

J. Kere, S. Katayama, K. Krjutškov, 2016, PloS one.