KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences

INTRODUCTION: Long QT Syndrome (LQTS) is an inherited disease with an abnormal electrical conduction system in the heart that can cause sudden death as a result of QT prolongation. LQT2 is the second most common subtype of LQTS caused by loss of function mutations in the potassium voltage-gated chan...

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Detalles Bibliográficos
Autores principales: Ke, ZunPing, Li, Chao, Bai, Gang, Tan, Li, Wang, JunFeng, Zhou, Ming, Zhou, JianHua, Chen, Shi-You, Dong, Xiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562146/
https://www.ncbi.nlm.nih.gov/pubmed/37783170
http://dx.doi.org/10.1016/j.clinsp.2023.100285

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562146/
https://www.ncbi.nlm.nih.gov/pubmed/37783170
http://dx.doi.org/10.1016/j.clinsp.2023.100285

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