Bibliographic Details
| 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. |
| Database: |
Academic Search Ultimate |
