Cite
HARVARD Citation
Kiuchi, Z. et al. (2023). Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type II. JCEM case reports. 1 (2), p. . [Online].
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Kiuchi, Z. et al. (2023). Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type II. JCEM case reports. 1 (2), p. . [Online].