Somatic mutations in children with GATA2-associated myelodysplastic syndrome who lack other features of GATA2 deficiency

Abstract excerpt

Key Points Children with primary MDS should be tested for GATA2 mutations, regardless of karyotype, family history, or features of GATA2 deficiency. Screening children with GATA2-MDS for somatic mutations may reveal mutations predictive of clinical outcomes.

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