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Göran Carlsson, Malin Melin, Niklas Dahl, Kim Göransdotter Ramme, Magnus Nordenskjöld, Jan Palmblad, Jan-Inge Henter and Bengt Fadeel Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia Acta Paediatrica 96

Article first published online: 24 MAY 2007 | DOI: 10.1111/j.1651-2227.2007.00274.x

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