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EMMM.201505444
EMMM.201505444
http://dx.doi.org/10.15252/EMMM.201505444
Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia.
P356
Q36159459-AC2394B9-48B8-4D26-807D-21C1CF895870
P356
EMMM.201505444
http://dx.doi.org/10.15252/EMMM.201505444