Figure 6

![Figure 6: Genetic variant analysis from the Bartter syndrome case series reveals the molecular basis underlying different clinical presentations. The wide variety of pathogenic mutations affects distinct ion transport channels in the renal tubule.]()

> Source: Rakhtan K Qasba et al. "Bartter Syndrome: A Systematic Review of Case Reports and Case Series.." *Medicina (Kaunas, Lithuania)*, 2023. PMID: [37763757](https://pubmed.ncbi.nlm.nih.gov/37763757/)

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  <img src="" alt="Genetic variant analysis from the Bartter syndrome case series reveals the molecular basis underlying different clinical presentations. The wide variety of pathogenic mutations affects distinct ion transport channels in the renal tubule." />
  <figcaption>Figure 6. Genetic variant analysis from the Bartter syndrome case series reveals the molecular basis underlying different clinical presentations. The wide variety of pathogenic mutations affects distinct ion transport channels in the renal tubule.<br>  Source: Rakhtan K Qasba et al. "Bartter Syndrome: A Systematic Review of Case Reports and Case Series.." <em>Medicina (Kaunas, Lithuania)</em>, 2023. PMID: <a href="https://pubmed.ncbi.nlm.nih.gov/37763757/">37763757</a></figcaption>
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