Characterisation of the Cullin‐3 mutation that causes a severe form of familial hypertension and hyperkalaemia-Reference-Cited by-同舟云学术

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

Published:2015-08-18 Issue:10 Volume:7 Page:1285-1306
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Schumacher Frances‐Rose¹,Siew Keith²,Zhang Jinwei¹,Johnson Clare¹,Wood Nicola¹,Cleary Sarah E²,Al Maskari Raya S²,Ferryman James T²,Hardege Iris²,Yasmin ²,Figg Nichola L³,Enchev Radoslav⁴,Knebel Axel¹,O'Shaughnessy Kevin M²,Kurz Thimo¹

Affiliation:

1. MRC Protein Phosphorylation and Ubiquitylation Unit College of Life Sciences University of Dundee Dundee UK

2. Division of Experimental Medicine and Immunotherapeutics University of Cambridge Cambridge UK

3. Division of Cardiovascular Medicine Department of Medicine University of Cambridge Cambridge UK

4. Institute of Biochemistry ETH Zürich Zürich Switzerland

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201505444

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