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. 2016 Nov 1;55(21):3201–3204. doi: 10.2169/internalmedicine.55.6390

Figure 2.

Figure 2.

Sanger sequencing of all exon regions of SLC12A3 revealed a heterozygous mutation in c.C3052T, which changes the codon of the 1,018th arginine to a stop codon. No additional mutation was found.