MYD88 mutated and wild-type waldenström’s macroglobulinemia: Characterization of chromosome 6q gene losses and their mutual exclusivity with mutations in CXCR4
Academic Article
Publication Date:
2018
Iris type:
1.1 Articolo in rivista
Keywords:
Biomarkers; Genetic Association Studies; Humans; Myeloid Differentiation Factor 88; Receptors, CXCR4; Waldenstrom Macroglobulinemia; Chromosome Deletion; Mutation
List of contributors:
Guerrera, M. L.; Tsakmaklis, N.; Xu, L.; Yang, G.; Demos, M.; Kofides, A.; Chan, G. G.; Manning, R. J.; Liu, X.; Chen, J. G.; Munshi, M.; Patterson, C. J.; Castillo, J. J.; Dubeau, T.; Gustine, J.; Carrasco, R. D.; Arcaini, L.; Varettoni, M.; Cazzola, M.; Treon, S. P.; Hunter, Z. R.
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