Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia
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J. Palmblad | B. Fadeel | M. Nordenskjöld | N. Dahl | J. Henter | G. Carlsson | M. Melin | K. Ramme | Kim Göransdotter Ramme | Kim Göransdotter Ramme
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