Highlight: Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
We would like to draw your attention to this case report published in HeartRhythmn Case Reports in May 2016, which Prof. Luc Jordaens selected as being of particular interest to our membership.
You can read the full case report at this link.
Authors: Anders KroghBroendberg, MD* Lisbeth NoerumPedersen, MSc, PhD† Jens Cosedis Nielsen, MD, DMSc, PhD* Henrik KjaerulfJensen, MD, DMSc, PhD*
*Department of Cardiology and †Department of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark