A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia

Fan, P; Zhao, YM; Zhang, D; Liao, Y; Yang, KQ; Tian, T; Lou, Y; Luo, F; Ma, WJ; Zhang, HM; Song, L; Cai, J; Liu, YX; Zhou, XL

Liu, YX (reprint author), Peking Union Med Coll, Beijing, Peoples R China.; Liu, YX (reprint author), Chinese Acad Med Sci, Natl Ctr Cardiovasc Dis, Fuwai Hosp, Dept Emergency & Crit Care Ctr, Beijing, Peoples R China.

AMERICAN JOURNAL OF HYPERTENSION, 2019; 32 (8): 752

Abstract

BACKGROUND Liddle syndrome (LS) is an autosomal dominant disorder caused by single-gene mutations of the epithelial sodium channel (ENaC). It is chara......

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