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Göran Carlsson, Göran Elinder, Helena Malmgren, Alicja Trebinska, Ewa Grzybowska, Niklas Dahl, Magnus Nordenskjöld and Bengt Fadeel Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities Pediatric Blood & Cancer 53

Article first published online: 4 JUN 2009 | DOI: 10.1002/pbc.22131

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