1. Apparent mineralocorticoid excess caused by novel compound heterozygous mutations in HSD11B2. (25th November 2020) Authors: Fan, P; Zhang, D; Yang, K.Q; Zhang, Y; Lu, Y.T; Luo, F; Tian, T; Liu, Y.X; Zhou, X.L Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical genetics involved in monogenic forms of hypertension in Chinese patients with early-onset hypertension and hypokalemia. (25th November 2020) Authors: Fan, P; Zhang, D; Yang, K.Q; Zhang, Y; Lu, Y.T; Luo, F; Tian, T; Liu, Y.X; Zhou, X.L Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗