Rarity and phenotypic heterogeneity provide challenges in the diagnosis of Andersen-Tawil syndrome: Two cases presenting with ECGs mimicking catecholaminergic polymorphic ventricular tachycardia (CPVT)

Tully, I., Atherton, J., Hunt, L., Ingles, J., Semsarian, C. and McGaughran, J. (2015) Rarity and phenotypic heterogeneity provide challenges in the diagnosis of Andersen-Tawil syndrome: Two cases presenting with ECGs mimicking catecholaminergic polymorphic ventricular tachycardia (CPVT). International Journal of Cardiology, 201 473-475. doi:10.1016/j.ijcard.2015.07.069


Author Tully, I.
Atherton, J.
Hunt, L.
Ingles, J.
Semsarian, C.
McGaughran, J.
Title Rarity and phenotypic heterogeneity provide challenges in the diagnosis of Andersen-Tawil syndrome: Two cases presenting with ECGs mimicking catecholaminergic polymorphic ventricular tachycardia (CPVT)
Journal name International Journal of Cardiology   Check publisher's open access policy
ISSN 0167-5273
1874-1754
Publication date 2015-12-01
Year available 2015
Sub-type Letter to editor, brief commentary or brief communication
DOI 10.1016/j.ijcard.2015.07.069
Open Access Status Not Open Access
Volume 201
Start page 473
End page 475
Total pages 3
Place of publication Shannon, Clare, Ireland
Publisher Elsevier Ireland
Language eng
Keyword Arrhythmia
Arrest
Andersen-Tawil Syndrome
Kcnj2
CPVT periodic paralysis
Q-Index Code CX
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Letter to editor, brief commentary or brief communication
Collections: Non HERDC
School of Medicine Publications
 
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