The Relationship Between FLT3 Mutations And Complete Remission Of AML Patients Referring To Shariati Hospital
Background and Aim: FLT3 gene is a member of class III receptor Tyrosine Kinase, which is expressed in most patients with acute myeloid leukemia (AML). Mutations of FLT3 such as Internal Tandem Duplication (ITD) and point mutation of the D835 are the most common genetic defects in myeloid leukemia....
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| Main Authors: | , , |
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| Format: | Book |
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Tehran University of Medical Sciences,
2013-09-01T00:00:00Z.
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