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RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML

Key Points. Germline RUNX1 mutations lead to significant phenotypic heterogeneity in families.Germline RUNX1-mutated acute myeloid leukemia has a different som

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Bibliographic Details
Main Authors: Brown, Anna L. (Author) , Bochtler, Tilmann (Author) , Fröhling, Stefan (Author)
Format: Article (Journal)
Language:English
Published: 24 March 2020
In: Blood advances
Year: 2020, Volume: 4, Issue: 6, Pages: 1131-1144
ISSN:2473-9537
DOI:10.1182/bloodadvances.2019000901
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1182/bloodadvances.2019000901
Verlag, lizenzpflichtig, Volltext: https://ashpublications.org/bloodadvances/article/4/6/1131/452758/RUNX1-mutated-families-show-phenotype
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Author Notes:Anna L. Brown, Peer Arts, Catherine L. Carmichael, Milena Babic, Julia Dobbins, Chan-Eng Chong, Andreas W. Schreiber, Jinghua Feng, Kerry Phillips, Paul P. S. Wang, Thuong Ha, Claire C. Homan, Sarah L. King-Smith, Lesley Rawlings, Cassandra Vakulin, Andrew Dubowsky, Jessica Burdett, Sarah Moore, Grace McKavanagh, Denae Henry, Amanda Wells, Belinda Mercorella, Mario Nicola, Jeffrey Suttle, Ella Wilkins, Xiao-Chun Li, Joelle Michaud, Peter Brautigan, Ping Cannon, Meryl Altree, Louise Jaensch, Miriam Fine, Carolyn Butcher, Richard J. D’Andrea, Ian D. Lewis, Devendra K. Hiwase, Elli Papaemmanuil, Marshall S. Horwitz, Georges Natsoulis, Hugh Y. Rienhoff, Nigel Patton, Sally Mapp, Rachel Susman, Susan Morgan, Julian Cooney, Mark Currie, Uday Popat, Tilmann Bochtler, Shai Izraeli, Kenneth Bradstock, Lucy A. Godley, Alwin Krämer, Stefan Fröhling, Andrew H. Wei, Cecily Forsyth, Helen Mar Fan, Nicola K. Poplawski, Christopher N. Hahn, and Hamish S. Scott
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Summary:Key Points. Germline RUNX1 mutations lead to significant phenotypic heterogeneity in families.Germline RUNX1-mutated acute myeloid leukemia has a different som
Item Description:Gesehen am 23.04.2020
Physical Description:Online Resource
ISSN:2473-9537
DOI:10.1182/bloodadvances.2019000901

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