This case report in Blood Cells, Molecules and Diseases describes a patient with myelofibrosis who was sequenced with our hematopoietic disorders gene set. Analysis revealed very rare, concurrent pathogenic mutations in MPL.
Concurrent MPLW515L and Y591D mutations in a patient with myelofibrosis. Rashidi A, Heusel JW, Oh ST. Blood Cells Mol Dis. 60 (2016) 1-2. Read the article.
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