Cite
MLA Citation
Yohan Bignon et al.. “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.” Human mutation, vol. 41, no. 4, 2020, pp. 774–785. http://access.bl.uk/ark:/81055/vdc_100102543369.0x000040