Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

BACKGROUND: Phenotypic overlap of type 3 long QT syndrome (LQT3), Brugada syndrome (BrS), cardiac conduction disease (CCD), and sinus node dysfunction (SND) is observed with SCN5A mutations. SCN5A‐E1784K is the most common mutation associated with BrS and LQTS3. The present study examines the genoty...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:J Am Heart Assoc
Huvudupphovsmän: Veltmann, Christian, Barajas‐Martinez, Hector, Wolpert, Christian, Borggrefe, Martin, Schimpf, Rainer, Pfeiffer, Ryan, Cáceres, Gabriel, Burashnikov, Elena, Antzelevitch, Charles, Hu, Dan
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2016
Ämnen:
Original Research
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5015375/
https://ncbi.nlm.nih.gov/pubmed/27381756
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/JAHA.116.003379
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk