Cargando…
A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes
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 syncope...
Autores principales: | Touat-Hamici, Zahia, Blancard, Malorie, Ma, Ruifang, Lin, Lianyun, Iddir, Yasmine, Denjoy, Isabelle, Leenhardt, Antoine, Yuchi, Zhiguang, Guicheney, Pascale |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970841/ https://www.ncbi.nlm.nih.gov/pubmed/33664309 http://dx.doi.org/10.1038/s41598-021-84373-9 |
Ejemplares similares
-
A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response
por: Blancard, Malorie, et al.
Publicado: (2021) -
Crystal structures of ryanodine receptor SPRY1 and tandem-repeat domains reveal a critical FKBP12 binding determinant
por: Yuchi, Zhiguang, et al.
Publicado: (2015) -
Structural Insight Into Ryanodine Receptor Channelopathies
por: Hadiatullah, Hadiatullah, et al.
Publicado: (2022) -
An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation
por: Blancard, Malorie, et al.
Publicado: (2018) -
Interplay between Selenium Levels and Replicative Senescence in WI-38 Human Fibroblasts: A Proteomic Approach
por: Hammad, Ghania, et al.
Publicado: (2018)