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. 2015 Feb 20;19(4):806–814. doi: 10.1111/jcmm.12497

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© 2015 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.

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Fig 3 — Sequence analysis of mutations underlying Wilson's disease. DNA from WD patients were isolated and sequenced by standard procedures. Individual mutations sites are indicated by asterisks. The numbering of nucleotides is given according to GenBank entry with accession no. U03464.1 starting with the translational start codon (ATG) at position +1. The nucleotide substitutions at position +2332, +2930, +3207, and +3784 result in nonsynonymous amino acid exchanges at position 778 (R778G), 977 (T977M), 1069 (H1069Q) and 1262 (V1262F) respectively.