BC5756D7-0DAF-4A37-ACE1-E3A0F3304A49Determining the causal links and clinical significance of rare genetic variantsFellowshipMR/R026408/1C008C651-F5B0-4859-A334-5F574AB6B57CMRCINCOME_ACTUAL25465750E36136-3EFA-47B0-A393-E38168AFE431An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.Scientific reports3f939a16af5cbf59c3d6ff32ff0cf954Kerr SM2019-01-01http://dx.doi.org/10.1038/s41598-019-47436-631358886http://ukpmc.ac.uk/abstract/MED/313588862045-2322http://europepmc.org/abstract/MED/3135888691Journal Article/Review5e61085e4651d4.28708022