Publications: The RUNX1 Database (RUNX1db): Establishment of an Expert Curated RUNX1 Registry and Genomics Database as a Public Resource for Familial Platelet Disorder with Myeloid MalignancySecondary Leukemia in Patients with Germline Transcription Factor Mutations (RUNX1, GATA2, CEBPA)RUNX1-mutated Families Show Phenotype Heterogeneity and a Somatic Mutation Profile Unique to Germline Predisposed AML
