O.K. Steinlein
Institute of Human Genetics
Rheinische Friedrich Wilhelms-Universität
D-53111
Germany
Name/email consistency: high
- Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy. Steinlein, O.K., Neubauer, B.A., Sander, T., Song, L., Stoodt, J., Mount, D.B. Epilepsy Res. (2001)