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- W3148672162 abstract "Brugada syndrome is a rare inherited arrhythmia with high risk of sudden cardiac death. We present the findings for a molecular convergence of clinically relevant mutations and identification of a single-cell transcriptome-derived cardiac cell types that are associated with the etiology of BrS. Our study suggests that genomic and proteomic hotspots in BrS converge into ion transport pathway and cardiomyocyte as a major BrS-associated cell type that provides insight into the complex genetic etiology of BrS." @default.
- W3148672162 created "2021-04-13" @default.
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- W3148672162 date "2021-05-01" @default.
- W3148672162 modified "2023-10-14" @default.
- W3148672162 title "Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome" @default.
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- W3148672162 doi "https://doi.org/10.1152/ajpheart.00061.2021" @default.
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