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. 2020 Aug 8;8(10):e1428. doi: 10.1002/mgg3.1428

Figure 1.

Figure 1

Electropherogram of Sanger sequencing results of the intronic variant NG_008806.1 (ATP7B_v001):c.2866‐1521G>A in ATP7B (the mutated site is heterozygous). All predictive software showed creation of an acceptor splicing site in this variant