1.
Agarwal K, Shankar GH, Sarangi B, Walimbe A. Compound heterozygote KCNQ1 mutation causing Jervell Lange Neilson syndrome: a case report of genotype-phenotype correlation. Int J Contemp Pediatr [Internet]. 2021 Jun. 24 [cited 2025 Oct. 25];8(7):1307-9. Available from: https://www.ijpediatrics.com/index.php/ijcp/article/view/4281