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High prevalence of genetic variants previously associated with LQT syndrome in new exome data
Lena Refsgaard, Anders G Holst, Golnaz Sadjadieh, Stig Haunsø, Jonas B Nielsen,
Morten S Olesen
Institut for Klinisk Medicin
Undervisning
Molecular Cardiology and Membrane Proteins
101
Citationer (Scopus)
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Biochemistry, Genetics and Molecular Biology
Genetic Divergence
100%
Exome
100%
Long QT Syndrome
100%
Prevalence
100%
Exome Sequencing
90%
Population Dynamics
20%
Genotyping
10%
Missense
10%
Population Research
10%
Genetic Variation
10%
Population
10%
Allele
10%
Keyphrases
High Prevalence
100%
Genetic Variants
100%
Exome
100%
Long QT Syndrome
100%
Control Population
20%
PolyPhen-2
20%
Published Data
10%
Genetic Variation
10%
Cav1.3
10%
Population-based Study
10%
Disease Causation
10%
Family Members
10%
SCN5A
10%
NHLBI
10%
Risk Stratification
10%
Missense Variants
10%
Functional Impact
10%
KCNH2
10%