Characterisation of the Cullin‐3 mutation that causes a severe form of familial hypertension and hyperkalaemia

Publisher： John Wiley & Sons Inc

E-ISSN： 1757-4684|7|10|1285-1306

ISSN： 1757-4676

Source： EMBO Molecular Medicine, Vol.7, Iss.10, 2015-10, pp. : 1285-1306

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