Case Report
Copyright ©The Author(s) 2019.
World J Clin Cases. Sep 6, 2019; 7(17): 2630-2636
Published online Sep 6, 2019. doi: 10.12998/wjcc.v7.i17.2630
Figure 1
Figure 1 Wilson disease patient’s family pedigree showing the mutations detected in ATP7B. A: The family pedigree. The arrow indicates the proband; her parents had no signs of Wilson disease; B: Non-synonymous mutations detected in the family. The proband had both mutations, while the c.3809A>G mutation was only detected in her mother and the c.2333G>T mutation was only detected in her father.