Christoph Klein
Department of Pediatric Hematology/Oncology
Hannover Medical School
Germany
Name/email consistency: high
- Genetic defects in severe congenital neutropenia: emerging insights into life and death of human neutrophil granulocytes. Klein, C. Annu. Rev. Immunol. (2011)
- Genetic insights into congenital neutropenia. Klein, C., Welte, K. Clin. Rev. Allergy. Immunol (2010)
- 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)