Figure 2.

Chromatograms of 58 novel ATP7B variants identified in the present study. The lower chromatogram in each frame represents the variant, while the upper one represents the normal sequence. The c.4162delG variant is shown in reverse sequence, while the other 57 variants are illustrated in forward sequence. 2A, 2B, 2C and 2D respectively illustrates 32 missense changes, 16 small deletions or insertions, 6 splicing site variants as well as 4 nonsense variants.