Associated Papers
In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening.
Louet M et al.
Scientific Reports, 2017
ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
Andrini O et al.
American Journal of Physiology. Renal Physiology, 2015
Patients with biallelic mutations in the chloride channel gene CLCNKB: long-term management and outcome.
Bettinelli A et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation, 2007
Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.
Konrad M et al.
Journal of the American Society of Nephrology : Jasn, 2000
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