Associated Papers
ClC-K Kidney Chloride Channels: From Structure to Pathology.
Andrini O et al.
Handbook of Experimental Pharmacology, 2024
Analysis of CLCNKB mutations at dimer-interface, calcium-binding site, and pore reveals a variety of functional alterations in ClC-Kb channel leading to Bartter syndrome.
Bignon Y et al.
Human Mutation, 2020
Monogenic causes of chronic kidney disease in adults.
Connaughton DM et al.
Kidney International, 2019
In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening.
Louet M et al.
Scientific Reports, 2017
Clinical and Genetic Spectrum of Bartter Syndrome Type 3.
Seys E et al.
Journal of the American Society of Nephrology : Jasn, 2017
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