Whole genome sequencing of families diagnosed with cardiac channelopathies reveals structural variants missed by whole exome sequencing-Reference-Cited by-同舟云学术

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

Published:2024-06-18 Issue:9 Volume:69 Page:455-465
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Senthivel Vigneshwar^ORCID,Jolly Bani,VR Arvinden,Bajaj Anjali,Bhoyar Rahul,Imran Mohamed,Vignesh Harie,Divakar Mohit Kumar^ORCID,Sharma Gautam,Rai Nitin,Kumar Kapil,MP Jayakrishnan,Krishna Maniram,Shenthar Jeyaprakash,Ali Muzaffar,Abqari Shaad,Nadri Gulnaz,Scaria Vinod,Naik Nitish,Sivasubbu Sridhar

Funder

Council of Scientific and Industrial Research

Indian Council of Medical Research

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s10038-024-01265-2.pdf

Reference54 articles.

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