Novel combinations of variations in KCNQ1 were associated with patients with long QT syndrome or Jervell and Lange-Nielsen syndrome

OBJECTIVES: Long QT syndrome (LQTS) is one of the primary causes of sudden cardiac death (SCD) in youth. Studies have identified mutations in ion channel genes as key players in the pathogenesis of LQTS. However, the specific etiology in individual families remains unknown. METHODS: Three unrelated...

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Detalles Bibliográficos
Autores principales: Zhao, Nongnong, Yu, Zhengyang, Cai, Zhejun, Chen, Wenai, He, Xiaopeng, Huo, Zhaoxia, Lin, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422715/
https://www.ncbi.nlm.nih.gov/pubmed/37568094
http://dx.doi.org/10.1186/s12872-023-03417-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422715/
https://www.ncbi.nlm.nih.gov/pubmed/37568094
http://dx.doi.org/10.1186/s12872-023-03417-2

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