HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
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Bengt Fadeel | Bodo Grimbacher | Alejandro A Schäffer | Christoph Klein | Nima Rezaei | Göran Carlsson | Kaan Boztug | A. Schäffer | J. Palmblad | C. Klein | B. Fadeel | K. Welte | N. Rezaei | B. Grimbacher | I. Sandrock | N. Dahl | M. Germeshausen | M. Grudzień | Georg Bohn | J. Henter | K. Boztug | Manuela Germeshausen | Karl Welte | Georg Bohn | Niklas Dahl | Magda Grudzien | Cornelia Zeidler | B. Schwinzer | C. Rathinam | G. Carlsson | Jan Palmblad | Jan-Inge Henter | Giridharan Appaswamy | Inga Sandrock | Chozhavendan Rathinam | Beate Schwinzer | Malin Melin | C. Zeidler | M. Melin | Giridharan Appaswamy
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