The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele
Many rare high-impact variants have been associated with disease, but the origins and functional impact are not always explored. Here, the authors trace the ancestry of a rare high impact atrial fibrillation allele in KCNQ1, and use iPSC-derived cardiomyocytes to characterize the effect of the allel...
Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Médium: | Článek |
Jazyk: | English |
Vydáno: |
Nature Portfolio
2021-11-01
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Edice: | Nature Communications |
On-line přístup: | https://doi.org/10.1038/s41467-021-26741-7 |