Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleAnalysis 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.AuthorsBignon, Yohan; Sakhi, Imene; Bitam, Sara; Bakouh, Naziha; Keck, Mathilde; Frachon, Nadia; Paulais, Marc; Planelles, Gabrielle; Teulon, Jacques; Andrini, OlgaPublicationHuman Mutation, 2020, Vol 41, Issue 4, p774ISSN1059-7794Publication typeArticleDOI10.1002/humu.23962