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Author/Creator Sakhi, Imene

1. 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. Issue 4 (24th December 2019)

Authors:
Bignon, Yohan; Sakhi, Imene; Bitam, Sara; Bakouh, Naziha; Keck, Mathilde; Frachon, Nadia; Paulais, Marc; Planelles, Gabrielle; Teulon, Jacques; Andrini, Olga
Journal:
Human mutation
Issue:
Volume 41:Issue 4(2020)
Page Start:
774
Record Type:
Journal Article
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