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. 2016 Nov 30;59(Suppl 1):S157–S160. doi: 10.3345/kjp.2016.59.11.S157

Fig. 3. Genetic analysis showing that the patient had a heterozygous mutation, c.649_650insC, in the proline-rich transmembrane protein-2 (PRRT2) gene.

Fig. 3