Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen-Tawil syndrome

Ördög Balázs and Hategan Lídia and Kovács Mária and Seprényi György and Kohajda Zsófia and Nagy István and Hegedűs Zoltán and Környei László and Jost Norbert László and Jancsó Gáborné Katona Márta and Szekeres Miklós and Forster Tamás and Papp Gyula and Varró András and Sepp Róbert: Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen-Tawil syndrome.
Canadian journal of physiology and pharmacology, 93 (7). pp. 569-575. ISSN 1205-7541 (2015)

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Item Type: Journal Article
Journal or Publication Title: Canadian journal of physiology and pharmacology
Date: 2015. July
Volume: 93
Number: 7
Page Range: pp. 569-575
ISSN: 1205-7541
Faculty/Unit: Faculty of Medicine
Institution: Szegedi Tudományegyetem
Language: English
MTMT rekordazonosító: 2912613
DOI azonosító: https://doi.org/10.1139/cjpp-2014-0527
Date Deposited: 2017. May. 04. 17:14
Last Modified: 2019. Oct. 17. 13:40
URI: http://publicatio.bibl.u-szeged.hu/id/eprint/9043
Web of Science® Times Cited: 3 View citing articles in Web of Science®

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