Role for germline mutations and a rare coding single nucleotide polymorphism within the KCNJ5 potassium channel in a large cohort of sporadic cases of primary aldosteronism
种系突变和 KCNJ5 钾通道中罕见编码单核苷酸多态性在大量散发原发性醛固酮增多症病例中的作用
期刊:Hypertension
影响因子:6.9
doi:10.1161/HYPERTENSIONAHA.113.02234
Meena Murthy, Shengxin Xu, Gianmichele Massimo, Martin Wolley, Richard D Gordon, Michael Stowasser, Kevin M O'Shaughnessy