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Sequences of CEBPA mutations at diagnosis of AML. (A) Germline N-terminal frameshift CEBPA 19-base pair deletion (c.147_165del, p.Glu50fs). (B) Identical somatic C-terminal an inframe insertion of aminoacid lysine (c.936_937dupAAG, p.313_314insLys). (C) An inframe deletion of 50 aminoacids (c.911_1060del, p.304-353del) present at diagnosis only in twin A.
