Fig. 1From: Novel mutation in the SLC12A3 gene in a Sri Lankan family with Gitelman syndrome & coexistent diabetes: a case reportPartial electropherograms from exon 10 of the SLC12A3 gene showing a homozygous missense mutation from A to T at nucleotide position 1276 [NM_000339.2, c.1276A > T; p.N426Y] in the proband (a) and the corresponding heterozygous mutation in the mother (b)Back to article page