Characterisation of the Cullinâ•'3 mutation that causes a severe form of familial hypertension and hyperkalaemia
Characterisation of the Cullinâ•'3 mutation that causes a severe form of familial hypertension and hyperkalaemia
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Expression of Concern: Abstracts - 2019 - Basic & Clinical Pharmacology & Toxicology - Wiley Online Library
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Characterisation of the Cullinâ•'3 mutation that causes a severe form of familial hypertension and hyperkalaemia
Meta-heterogeneity: Evaluating and Describing the Diversity in Glycosylation Between Sites on the Same Glycoprotein - ScienceDirect
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