HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
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| Description | scientific article |
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author: Jan Palmblad Bengt Fadeel Nima Rezaei Bodo Grimbacher Jan-Inge Henter Alejandro A Schäffer |
| Publication date | January 2007 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |