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Autor:
Manogna Das Oravakandy, Faiq Ahmed, Rachna Khera, Manasi Mundada, Sudha S. Murthy, Senthil J. Rajappa, M. V. T. Krishna Mohan, B. Pavan Kumar, A. Santa
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 38(4)
Nucleophosmin (NPM1) mutation is one of the most common recurring genetic abnormalities seen in acute myeloid leukemia (AML). Immunohistochemistry serves as a cost effective and simple surrogate testing method for detection of NPM1 mutation. This stu