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.
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.