Associated Papers
AKAP9-Related Channelopathy: Novel Pathogenic Variant and Review of the Literature.
Huynh MT et al.
Genes, 2022
Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young.
Jaouadi H et al.
Herz, 2021
Large next-generation sequencing gene panels in genetic heart disease: yield of pathogenic variants and variants of unknown significance.
van Lint FHM et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation, 2019
30847666 (PubMed )
Supplement: 12471_2019_1250_MOESM2_ESM.xlsx › Blad1
Gene-Targeted Analysis of Clinically Diagnosed Long QT Russian Families.
Maltese PE et al.
International Heart Journal, 2017
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