Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome

Overview of attention for article published in Journal of Physiology, June 2017

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RT @JPhysiol: Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome https://t.co/P…

Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome https://t.co/PNRfcyoiMI

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