Whole genome sequencing of families diagnosed with cardiac channelopathies reveals structural variants missed by whole exome sequencing

作者：Vigneshwar Senthivel, Bani Jolly, Arvinden VR, Anjali Bajaj, Rahul C. Bhoyar, Mohamed Imran, Harie Vignesh, Mohit Kumar Divakar, Gautam Sharma, Nitin Rai, Kapil Kumar, Jayakrishnan MP, Maniram Krishna, Jeyaprakash Shenthar, Muzaffar Ali, Shaad Abqari, Gulnaz Nadri, Vinod Scaria, Nitish Naik, Sridhar Sivasubbu · 发表于：Journal of Human Genetics · 年份：2024 · DOI：10.1038/s10038-024-01265-2 · 被引用次数：4 · 研究领域：Genomics and Rare Diseases、RNA and protein synthesis mechanisms、Cardiac electrophysiology and arrhythmias