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Paper Details

An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.
Sci Rep
11
2019
KCNH2, KCNH2 gene, LQTS, Long QT Syndrome, c.1750G, c.1750G>, haplotype, human, participant, participants, rare genetic variants, sequence variant, single nucleotide polymorphism, whole genome sequences
Author NameAffiliation
Caroline HaywardUniversity of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital
Alison MeynertUniversity of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital
Colin A SempleUniversity of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital
Colin A SempleUniversity of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital
Javier SantoyoThe Roslin Institute and R(D)SVS, University of Edinburgh
Veronique VitartUniversity of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital
James F WilsonUniversity of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital
James F WilsonUniversity of Edinburgh
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