Ke Z, Li C, Bai G, Tan L, Wang J, Zhou M, et al. KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences. Clinics [Internet]. 2023 Sep. 13 [cited 2025 Apr. 12];78:100285 . Available from: https://journals.usp.br/clinics/article/view/232219