An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. (2019)

First Author: Kerr SM

Attributed to: The Scottish Genomes Partnership funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41598-019-47436-6

PubMed Identifier: 31358886

Publication URI: http://europepmc.org/abstract/MED/31358886

Type: Journal Article/Review

Volume: 9

Parent Publication: Scientific reports

Issue: 1

ISSN: 2045-2322