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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

D-53111

Germany

[email]@uk.uni-bonn.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

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

References

  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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