Shared Senior Authorship.
Unusual functional manifestations of a novel STX11 frameshift mutation in two infants with familial hemophagocytic lymphohistiocytosis type 4 (FHL4)†
Version of Record online: 27 DEC 2010
Copyright © 2010 Wiley-Liss, Inc.
Pediatric Blood & Cancer
Volume 56, Issue 4, pages 654–657, April 2011
How to Cite
Macartney, C. A., Weitzman, S., Wood, S. M., Bansal, D., Steele, M., Meeths, M., Abdelhaleem, M. and Bryceson, Y. T. (2011), Unusual functional manifestations of a novel STX11 frameshift mutation in two infants with familial hemophagocytic lymphohistiocytosis type 4 (FHL4). Pediatr. Blood Cancer, 56: 654–657. doi: 10.1002/pbc.22676
Conflict of interest: Nothing to report.
- Issue online: 4 FEB 2011
- Version of Record online: 27 DEC 2010
- Manuscript Accepted: 5 MAY 2010
- Manuscript Received: 1 FEB 2010
- Swedish Society for Medical Research
- Mary Beve's Foundation
- David & Astrid Hagelen's Foundation
- Karolinska Institute Research Foundation
- Jonas Söderquist's Stipend
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