An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. (2019)
Attributed to:
Medical and Regulatory Genomics
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