Publication Details

Pubmed26286618
Title: Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia.
Year: 2015
DOI: https://doi.org/10.15252/emmm.201505444
First Author: Schumacher
Experimental setup: affinity chromatography technology (Biogrid)
enzymatic study (Biogrid)
pull down (Biogrid)
Throughput: Low Throughput (Biogrid)

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