We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleHAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).AuthorsKlein C; Grudzien M; Appaswamy G; Germeshausen M; Sandrock I; Schäffer AA; Rathinam C; Boztug K; Schwinzer B; Rezaei N; Bohn G; Melin M; Carlsson G; Fadeel B; Dahl N; Palmblad J; Henter JI; Zeidler C; Grimbacher B; Welte KPublicationNature genetics, 2007, Vol 39, Issue 1, p86ISSN1061-4036Publication typearticleDOI10.1038/ng1940