Clinical utility gene card for: Long-QT syndrome

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Bibliographic Details
Published inEuropean Journal of Human Genetics Vol. 29; no. 12; pp. 1825 - 1832
Main Authors Beckmann, Britt M, Scheiper-Welling, Stefanie, Wilde, Arthur A M, Kääb, Stefan, Schulze-Bahr, Eric, Kauferstein, Silke
Format Journal Article
LanguageEnglish
Published England Springer Science and Business Media LLC 01.12.2021
Nature Publishing Group
Springer International Publishing
Subjects
Causality
Clinical Utility Gene Card Update
ddc:610
Disease
Genes
Genetic Heterogeneity
Genetic Testing
Genetics
Genomes
Genomics
Genotype & phenotype
Heart
Hospitals
Humans
Ion Channels
Legal medicine
Long QT Syndrome
Long QT Syndrome/genetics [MeSH] ; Mutation [MeSH] ; Ion Channels/genetics [MeSH] ; Humans [MeSH] ; Genetic Heterogeneity [MeSH] ; Long QT Syndrome/diagnosis [MeSH] ; Clinical Utility Gene Card Update ; Genetics research ; Genetic Testing/standards [MeSH] ; Sensitivity and Specificity [MeSH] ; Cardiovascular diseases ; Phenotype [MeSH] ; Genetic Testing/methods [MeSH]
Mutation
Phenotype
Potassium
Sensitivity and Specificity
Validity
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Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1018-4813
1476-5438
1476-5438
DOI:10.1038/s41431-021-00904-y