Whole genome sequencing of families diagnosed with cardiac channelopathies reveals structural variants missed by whole exome sequencing.
Senthivel V, Jolly B, Vr A, Bajaj A, Bhoyar R, Imran M, Vignesh H, Divakar MK, Sharma G, Rai N, Kumar K, Mp J, Krishna M, Shenthar J, Ali M, Abqari S, Nadri G, Scaria V, Naik N, Sivasubbu S.
Senthivel V, et al.
J Hum Genet. 2024 Sep;69(9):455-465. doi: 10.1038/s10038-024-01265-2. Epub 2024 Jun 18.
J Hum Genet. 2024.
PMID: 38890497