Congenital long QT syndrome: a case report of LQT2 and LQT13 in a neonate

Journal article

Peer reviewed

Rachel Bond, Andrew Blaufox, Bruce Goldner and Apoor Patel

Europace (London, England), Vol.16(12), pp.1807-1807

12/01/2014

PMID: 25417227

Abstract

Electrocardiography - methods

ERG1 Potassium Channel

Ether-A-Go-Go Potassium Channels - genetics

Female

G Protein-Coupled Inwardly-Rectifying Potassium Channels - genetics

Genetic Predisposition to Disease - genetics

Humans

Infant, Newborn

Long QT Syndrome - classification

Long QT Syndrome - congenital

Long QT Syndrome - diagnosis

Polymorphism, Single Nucleotide - genetics

url

https://doi.org/10.1093/europace/euu299View

Published (Version of record) Open

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Title: Congenital long QT syndrome: a case report of LQT2 and LQT13 in a neonate
Creators: Rachel Bond - Hofstra University
Andrew Blaufox - Hofstra University
Bruce Goldner - Hofstra University
Apoor Patel - Hofstra North Shore, LIJ School of Medicine, Long Island, NY, USA
Publication Details: Europace (London, England), Vol.16(12), pp.1807-1807
Identifiers: 991006261162002656
Academic Unit: Cardiology
Language: English
Resource Type: Journal article