A family with Liddle's syndrome caused by a new c.1721 deletion mutation in the epithelial sodium channel β‑subunit-Reference-Cited by-同舟云学术

A family with Liddle's syndrome caused by a new c.1721 deletion mutation in the epithelial sodium channel β‑subunit

Published:2019-02-13 Issue: Volume: Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Ding Xia¹,Jia Na¹^ORCID,Zhao Cong¹,Zhong You¹,Dai Dapeng²,Zhao Yuanyuan³,Xu Chengqi³,Cai Jianping²,Wang Qing³,He Qing¹^ORCID

Affiliation:

1. Department of Cardiology, Beijing Hospital, National Center of Gerontology, Beijing 100730, P.R. China

2. The Key Laboratory of Geriatrics, Beijing Hospital and Beijing Institute of Geriatrics, Ministry of Health, Beijing 100730, P.R. China

3. Human Genome Research Center and College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, Hubei 430074, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

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1. A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review;Molecular Medicine Reports;2023-12-08

2. Summary of Known Genetic and Epigenetic Modification Contributed to Hypertension;International Journal of Hypertension;2023-05-09

3. A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension;Frontiers in Cardiovascular Medicine;2022-06-14

4. Function and Regulation of the Epithelial Na + Channel ENaC;Comprehensive Physiology;2021-06