Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome

Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome

Background: Liddle syndrome is an autosomal dominant form of monogenic hypertension. Phenotypic variability makes it difficult to identify patients with Liddle syndrome, resulting in misdiagnosis and severe complications at early age. Objectives: To identify mutation in SCNN1B and SCNN1G genes in an...

Full description

Bibliographic Details
Main Authors: Kun-Qi Yang, Chao-Xia Lu, Peng Fan, Ying Zhang, Xu Meng, Xue-Qi Dong, Fang Luo, Ya-Xin Liu, Hui-Min Zhang, Hai-Ying Wu, Jun Cai, Xue Zhang, Xian-Liang Zhou
Format: Article
Language:English
Published: Taylor & Francis Group 2018-02-01
Series:Clinical and Experimental Hypertension
Subjects:
early-onset hypertensive patients
liddle syndrome
mutation
sanger sequencing
scnn1b
scnn1g
Online Access:http://dx.doi.org/10.1080/10641963.2017.1334799

Internet

http://dx.doi.org/10.1080/10641963.2017.1334799

Similar Items