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
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| Description | scientific article published on 24 December 2019 |
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author: Olga Andrini Mathilde Keck Sara Bitam Imene B Sakhi Yohan Bignon |
| Publication date | December 24, 2019 |
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