Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia
Version of Record online: 24 MAY 2007
©2007 The Author(s)/Journal Compilation © 2007 Foundation Acta Pædiatrica/Acta Pædiatrica
Volume 96, Issue 6, pages 813–819, June 2007
How to Cite
Carlsson, G., Melin, M., Dahl, N., Ramme, K. G., Nordenskjöld, M., Palmblad, J., Henter, J.-I. and Fadeel, B. (2007), Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia. Acta Paediatrica, 96: 813–819. doi: 10.1111/j.1651-2227.2007.00274.x
- Issue online: 24 MAY 2007
- Version of Record online: 24 MAY 2007
- Received 23 January 2007; Revised: 11 February 2007; Accepted: 16 February 2007.
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