Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome - Yang, Kun-Qi; Lu, Chao-Xia; Fan, Peng; Zhang, Ying; Meng, Xu; Dong, Xue-Qi; Luo, Fang; Liu, Ya-Xin; Zhang, Hui-Min; Wu, Hai-Ying; Cai, Jun; Zhang, Xue; et al. (Clinical and experimental hypertension (1993), 2018)
Keywords: Age of Onset; Early-onset hypertensive patients; Epithelial Sodium Channels - genetics; Genetic Testing; Heterozygote; Humans; Hypertension - complications; Hypertension - drug therapy; Hypertension - genetics; Hypokalemia - complications; Liddle syndrome; Liddle Syndrome - diagnosis; Liddle Syndrome - genetics; Male; Mutation; Phenotype; Sanger sequencing; SCNN1B; SCNN1G; Young Adult; SCNN1G; mutation; Early-onset hypertensive patients; Sanger sequencing; Liddle syndrome; SCNN1B