A Novel Mutation in the KCNH2 Gene Associatedwith Long QT Syndrome: A Case Report.

Zha, Kelan; Ye, Qiang

Zha, Kelan; Ye, Qiang.

Affiliation

Zha K; Department of Cardiology, The Affiliated Hospital of Southwest Medical University, China.
Ye Q; Department of Cardiology, The Affiliated Hospital of Southwest Medical University, China art006023@yeah.net.

Ann Clin Lab Sci ; 51(2): 258-261, 2021 Mar.

Article in En | MEDLINE | ID: mdl-33941567

Subject(s)

ERG1 Potassium Channel/genetics; Long QT Syndrome/genetics; Adult; ERG1 Potassium Channel/metabolism; Electrocardiography; Family; Female; Genetic Testing; Humans; Long QT Syndrome/metabolism; Mutation; Pedigree; Torsades de Pointes/genetics; Torsades de Pointes/metabolism; Young Adult

Key words

KCNH2 gene; LQT2; long QT syndrome; mutation

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Long QT Syndrome / ERG1 Potassium Channel Type of study: Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans Language: En Journal: Ann Clin Lab Sci Year: 2021 Document type: Article Affiliation country: China Country of publication: United States

Search on Google

Add to My VHL

XML

PubMed Links