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

出版年份 2015 全文链接

标题

作者

关键词

出版物

Volume 7, Issue 10, Pages 1285-1306

出版商

EMBO

发表日期

2015-08-19

DOI

10.15252/emmm.201505444

Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.

Explore

Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.

Create Now