Open AccessA consistent arrhythmogenic trait in Brugada syndrome cellular phenotype
Author(s) -
Al Sayed Zeina R.,
Jouni Mariam,
Gourraud JeanBaptiste,
Belbachir Nadjet,
Barc Julien,
Girardeau Aurore,
Forest Virginie,
Derevier Aude,
Gaignerie Anne,
Chariau Caroline,
Cimarosti Bastien,
Canac Robin,
Olchesqui Pierre,
Charpentier Eric,
Schott JeanJacques,
Redon Richard,
Baró Isabelle,
Probst Vincent,
Charpentier Flavien,
Loussouarn Gildas,
Zibara Kazem,
Lamirault Guillaume,
Lemarchand Patricia,
Gaborit Nathalie
Publication year - 2021
Publication title -
clinical and translational medicine
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.125
H-Index - 1
ISSN - 2001-1326
DOI - 10.1002/ctm2.413
Subject(s) - brugada syndrome , phenotype , biology , medicine , channelopathy , genetics , gene
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom