Hereditary Leukemia Due to Rare <i>RUNX</i>1c Splice Variant (L472X) Pre

来源 :临床医学国际期刊(英文) | 被引量 : 0次 | 上传用户:zyff1985
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Deleterious mutations in the RUNX1 gene cause hereditary leukemia due to a rare syndrome called Familial platelet Disorder with Associated Myeloid Malignancy (FPDMM). We describe the characteristics of a family with FPDMM due to a novel RUNX1 mutation (L4
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