Takotsubo cardiomyopathy and congenital long QT syndrome in a patient with a novel duplication in the Per-Arnt-Sim (PAS) domain of hERG1.
| Data(s) |
2010
|
|---|---|
| Identificador |
http://serval.unil.ch/?id=serval:BIB_EB92CFC40B67 isbn:1556-3871[electronic], 1547-5271[linking] pmid:20004623 doi:10.1016/j.hrthm.2009.09.026 isiid:000276189400023 |
| Idioma(s) |
en |
| Fonte |
Heart Rhythm, vol. 7, no. 2, pp. 260-265 |
| Palavras-Chave | #Congenital Long QT Syndrome; HERG1; KCNH2; Takotsubo Cardiomyopathy; Voltage-Gated Potassium Channel; Repolarization; Mutations |
| Tipo |
info:eu-repo/semantics/article article |
