New SLC12A3 disease causative mutation of Gitelman’s syndrome

Figure 1 Electropherograms showing DNA sequences of exon 2 (A), exon 22 (B) and exon 23 (C), in the regions containing the variations detected.

Figure 2 Pedigree of family. Gitelman’s syndrome affected patients are colored in black, heterozygous carriers are filled in gray. Mutations and polymorphisms of subjects are reported close to their respective symbols.