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Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study

Genetic DisorderMedicineGeneticsPathologyChildhood AmlEuropean Multicenter StudyMolecular GeneticsDisease Gene IdentificationWt1 Gene MutationsGene ExpressionMolecular DiagnosticsInborn Error Of ImmunityVariant InterpretationClinical Genetics