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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

O.K. Steinlein

Institute of Human Genetics

Rheinische Friedrich Wilhelms-Universität




Name/email consistency: high



  • Institute of Human Genetics, Rheinische Friedrich Wilhelms-Universität, D-53111, Germany. 2001


  1. 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) [Pubmed]
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