Work

De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero

Year: 2005

Type: article

Study design: Case Report

Source: Cardiovascular Research

DOI: 10.1016/j.cardiores.2005.06.023

Authors: K HONG, D PIPER, A DIAZVALDECANTOS, J BRUGADA, A OLIVA, E BURASHNIKOV, J SANTOSDESOTO, J GRUESOMONTERO, E DIAZENFANTE, P BRUGADA, Frank Sachse, Michael C Sanguinetti, Ramon Brugada

Institutions: Masonic Medical Research Laboratory, University of Utah, Hospital Universitario Virgen del Rocío, Hospital Clínic de Barcelona

Language: English

Topic: Cardiac electrophysiology and arrhythmias

Subfield: Cardiology and Cardiovascular Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Heart, Lung, and Blood Institute

Awards: MOLECULAR GENETIC BASIS FOR FAMILIAL ATRIAL FIBRILLATION, SCOR IN SUDDEN CARDIAC DEATH

OpenAlex ID: W2025470533

FWCI: 13.84

Cites: 30

Cited by: 302

Related to: 10