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