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

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Title: HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
Authors: Klein, Christoph1 klein.christoph@mh-hannover.de, Grudzien, Magda2, Appaswamy, Giridharan1, Germeshausen, Manuela1, Sandrock, Inga1, Schäffer, Alejandro A.3, Rathinam, Chozhavendan1, Boztug, Kaan1, Schwinzer, Beate1, Rezaei, Nima4, Bohn, Georg1, Melin, Malin5, Carlsson, Göran6, Fadeel, Bengt7, Dahl, Niklas5, Palmblad, Jan8, Henter, Jan-Inge6, Zeidler, Cornelia1, Grimbacher, Bodo2, Welte, Karl1
Source: Nature Genetics. Jan2007, Vol. 39 Issue 1, p86-92. 7p. 1 Color Photograph, 1 Black and White Photograph, 1 Diagram, 1 Chart, 3 Graphs.
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  Data: HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
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  Data: <searchLink fieldCode="JN" term="%22Nature+Genetics%22">Nature Genetics</searchLink>. Jan2007, Vol. 39 Issue 1, p86-92. 7p. 1 Color Photograph, 1 Black and White Photograph, 1 Diagram, 1 Chart, 3 Graphs.
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