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

Ördög, Balázs, Hategan, Lídia, Kovács, Mária, Seprényi, György, Kohajda, Zsófia, Nagy, István, Hegedűs, Zoltán, Környei, László, Jost, Norbert László, Jancsó Gáborné Katona, Márta, Szekeres, Miklós, Forster, Tamás, Papp, Gyula, Varró, András, 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)

[img] Text
Ördög et al cjpp-2014-0527.pdf - Published Version
Restricted access: Registered users only

Download (1MB)
Item Type: 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: Faculty of Medicine
Institution: Szegedi Tudományegyetem
MTMT id: 2912613
DOI id: 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: 2 View citing articles in Web of Science®

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year