Rapid detection of DNMT3A R882 codon mutations allows early identification of poor risk patients with acute myeloid leukemia

Brewin, J. N., Horne, G. A. , Bisling, K. E., Stewart, H. J. and Chevassut, T. J. (2013) Rapid detection of DNMT3A R882 codon mutations allows early identification of poor risk patients with acute myeloid leukemia. Leukemia and Lymphoma, 54(6), pp. 1336-1339. (doi: 10.3109/10428194.2012.736986) (PMID:23035745)

Full text not currently available from Enlighten.

Abstract

No abstract available.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Horne, Dr Gillian
Authors: Brewin, J. N., Horne, G. A., Bisling, K. E., Stewart, H. J., and Chevassut, T. J.
College/School:College of Medical Veterinary and Life Sciences > School of Cancer Sciences
Journal Name:Leukemia and Lymphoma
Publisher:Taylor and Francis
ISSN:1042-8194
ISSN (Online):1029-2403

University Staff: Request a correction | Enlighten Editors: Update this record