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View article: Clinical and Genetic Spectrum of Bartter Syndrome Type 3
Clinical and Genetic Spectrum of Bartter Syndrome Type 3 Open
Bartter syndrome type 3 is a clinically heterogeneous hereditary salt-losing tubulopathy caused by mutations of the chloride voltage-gated channel Kb gene ( CLCNKB ), which encodes the ClC-Kb chloride channel involved in NaCl reabsorption …