Publication details

Four novel SCN5A mutations in patients with Brugada syndrome

Authors

BÉBAROVÁ Markéta JONGBLOED Roselie GEELEN Jan TIMMERMANS Carl ARENS Yvonne VOLDERS Paul RODRIGUEZ Luz-Maria

Year of publication 2006
Type Conference abstract
MU Faculty or unit

Faculty of Medicine

Citation
Description Four novel mutation in the SCN5A gene,coding the alpha-subunit of sodium channel, were detected in patients with Brugada syndrome.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info