Clinical and genetic analysis of multi-system pseudohypoaldosteronism
type 1 caused by a novel splice site mutation of the beta subunit gene
of epithelial sodium channel (ENaC)
- Sicui Hu
, - hongxiu yang,
- cheng Li,
- qiannan jiang,
- lingyan qiao,
- conghui hu,
- Tang Li
Abstract
This article aims to provide a comprehensive review of the clinical
features and genetics basis of multi-system pseudohypoaldosteronism type
1 caused by SCNN1B gene mutations.10 Dec 2020Submitted to Clinical Case Reports 12 Dec 2020Submission Checks Completed
12 Dec 2020Assigned to Editor
09 Jan 2021Reviewer(s) Assigned
16 Jan 2021Review(s) Completed, Editorial Evaluation Pending
21 Jan 2021Editorial Decision: Revise Minor
