HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

Authors: Christoph Klein, Magda Grudzien, Giridharan Appaswamy, Manuela Germeshausen, Inga Sandrock, Alejandro A. Schäffer, Chozhavendan Rathinam, Kaan Boztuǧ, Beate Schwinzer, Nima Rezaei, Georg Bohn, Malin Melin, Göran Carlsson, Bengt Fadeel, Niklas Dahl, Jan Palmblad, Jan‐Inge Henter, Cornelia Zeidler, Bodo Grimbacher, Karl Welte - Nature Genetics 2006 cited by 504