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HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
scientific article
Author/s
author: Jan-Inge Henter, Nima Rezaei, Jan Palmblad, Bengt Fadeel, Bodo Grimbacher, Alejandro A. Schäffer
Work details
Publication date
January 2007
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Language
English
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