HIGHLIGHTS
- who: Claus Meyer from the (UNIVERSITY) have published the article: Human MLL/KMT2A gene exhibits a second breakpoint cluster region for recurrent MLL⠍USP2 fusions, in the Journal: (JOURNAL)
- what: The authors sought to explore the involvement of rare germline genetic variants in susceptibility to MM. Within the discovery cohort of peripheral blood samples (see Supplementary Methods) from 66 individuals from 23 unrelated families analyzed by WES, DIS3 (NM_014953) was the only gene in which putative loss-of-function variants were observed in at least two families. The DIS3 variants discussed in this study are . . .
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