ASXL1 and STAG2 are Common Mutations in GATA2 Deficiency Patients with Bone Marrow Disease and Myelodysplastic Syndrome.
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DOI: 10.1182/bloodadvances.2021005065
Abstract: GATA2 Deficiency patients harbor de novo or inherited germline mutations in the GATA2 transcription factor gene, predisposing them to myeloid malignancies. There is considerable variation in disease progression, even among family members with the same… read more here.
Keywords: deficiency patients; mutations gata2; disease; somatic mutations ... See more keywords