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. Author manuscript; available in PMC: 2018 Mar 14.
Published in final edited form as: Mol Psychiatry. 2017 Sep 12;23(6):1487–1495. doi: 10.1038/mp.2017.179

Figure 1. A rare heterozygous nonsense mutation (C to T transition) was identified in a TD multiplex family by whole exome sequencing.

Figure 1

A. We performed whole exome sequencing on 4001, 4002, 5001, 5003 (proband), 5004 and 5005.

B. The heterozygous nonsense mutation at the PNKD gene was present in subjects 3001, 4001, 5001, 5003, 5004 and 5005.