Investigating the Complex Arrhythmic Phenotype Caused by the Gain-of-Function Mutation KCNQ1-G229D. (2019)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3389/fphys.2019.00259

PubMed Identifier: 30967788

Publication URI: http://europepmc.org/abstract/MED/30967788

Type: Journal Article/Review

Volume: 10

Parent Publication: Frontiers in physiology

ISSN: 1664-042X