Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous <i>SLC12A3</i> Mutations

<div>Sanger sequencing diagram of Pedigree B mutation type. (a) The Asp839Val (c.2516A&gt;T) heterozygous mutant type in <i>SLC12A3</i> exon21; (b) the corresponding wild type; (c) the NP_001119580.2:p.Arg904Gln (NM_001126108.2:c.2711G&gt;A, rs11643718) heterozygous mutant type in exon23; (d) the wild type at the corresponding position.</div>

BioMed Research International

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Figure 3: Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous <i>SLC12A3</i> Mutations 

Figure 3 | Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations 