A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes
Abstract Idiopathic ventricular fibrillation (IVF) causes sudden death in young adult patients without structural or ischemic heart disease. Most IVF cases are sporadic and some patients present with short-coupled torsade de pointes, the genetics of which are poorly understood. A man who had a first...
Guardado en:
Autores principales: | Zahia Touat-Hamici, Malorie Blancard, Ruifang Ma, Lianyun Lin, Yasmine Iddir, Isabelle Denjoy, Antoine Leenhardt, Zhiguang Yuchi, Pascale Guicheney |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/09050635e6e84eea9fe02cd858901af7 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes
por: Nabil El-Sherif, et al.
Publicado: (2019) -
Torsades de pointes in the PACU after outpatient endoscopy: a case report
por: Andrew Schaar, et al.
Publicado: (2021) -
Knockdown of SPRY4 and SPRY4-IT1 inhibits cell growth and phosphorylation of Akt in human testicular germ cell tumours
por: Mrinal K. Das, et al.
Publicado: (2018) -
Suppression of amiodarone‐induced torsade de pointes by landiolol in a patient with atrial fibrillation‐mediated cardiomyopathy
por: Koji Takahashi, et al.
Publicado: (2021) -
Phosphorylation of Ryanodine Receptors
por: DANILA,CRISTINA I, et al.
Publicado: (2004)