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Publikováno v:
OnLine Journal of Biological Sciences. 18:37-45
Since its discovery, mutations in NPM1 have been frequently associated with a large number of Acute Myeloid Leukemia (AML) patients. The vast majority of genetic changes were previously detected in exon 12, however little information report mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a92056de7600365d6c8ed0cff1d3cce5
https://doi.org/10.3844/ojbsci.2018.37.45
https://doi.org/10.3844/ojbsci.2018.37.45
