Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities
Version of Record online: 4 JUN 2009
Copyright © 2009 Wiley-Liss, Inc.
Pediatric Blood & Cancer
Volume 53, Issue 6, pages 1143–1146, 1 December 2009
How to Cite
Carlsson, G., Elinder, G., Malmgren, H., Trebinska, A., Grzybowska, E., Dahl, N., Nordenskjöld, M. and Fadeel, B. (2009), Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities. Pediatr. Blood Cancer, 53: 1143–1146. doi: 10.1002/pbc.22131
- Issue online: 9 SEP 2009
- Version of Record online: 4 JUN 2009
- Manuscript Accepted: 4 MAY 2009
- Manuscript Received: 6 MAR 2009
- Swedish Children's Cancer Foundation
- Swedish Cancer Foundation
- Swedish Research Council
- Stockholm County Council (ALF Project)
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