CCND2 mutations are infrequent events in BCR-ABL1 negative myeloproliferative neoplasm patients.
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DOI: 10.3324/haematol.2020.252643
Abstract: Classical or BCR-ABL1 negative myeloproliferative neoplasms (MPN) are clonal diseases originating from the acquisition at the stem cell level of a phenotype driver mutation affecting JAK2, MPL or CALR genes. MPN are comprised of three… read more here.
Keywords: ccnd2; ccnd2 mutations; gene; bcr abl1 ... See more keywords