Fig. 3From: A novel missense mutation in the MECOM gene in a Chinese boy with radioulnar synostosis with amegakaryocytic thrombocytopeniaMECOM: MDS1 and EVI1 complex locus on Chr 3q26.2. EVI1 gene and isoform were indicated. Location of patient variant indicated in red. NLS, nuclear localization sequence; CTBP, C-terminal-binding protein; AA, amino acidBack to article page