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

Christoph Klein

Department of Pediatric Hematology/Oncology

Hannover Medical School

Germany

[email]@mh-hannover.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Pediatric Hematology/Oncology, Hannover Medical School, Germany. 2007 - 2011

References

  1. Genetic defects in severe congenital neutropenia: emerging insights into life and death of human neutrophil granulocytes. Klein, C. Annu. Rev. Immunol. (2011) [Pubmed]
  2. Genetic insights into congenital neutropenia. Klein, C., Welte, K. Clin. Rev. Allergy. Immunol (2010) [Pubmed]
  3. HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Klein, C., Grudzien, M., Appaswamy, G., Germeshausen, M., Sandrock, I., Schäffer, A.A., Rathinam, C., Boztug, K., Schwinzer, B., Rezaei, N., Bohn, G., Melin, M., Carlsson, G., Fadeel, B., Dahl, N., Palmblad, J., Henter, J.I., Zeidler, C., Grimbacher, B., Welte, K. Nat. Genet. (2007) [Pubmed]
 
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