Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
HeartRhythm Case Rep
.
2016 Mar 9;2(3):261-264.
doi: 10.1016/j.hrcr.2016.02.008.
eCollection 2016 May.
Authors
Anders Krogh Broendberg
1
,
Lisbeth Noerum Pedersen
2
,
Jens Cosedis Nielsen
1
,
Henrik Kjaerulf Jensen
1
Affiliations
1
Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
2
Department of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark.
PMID:
28491684
PMCID:
PMC5419769
DOI:
10.1016/j.hrcr.2016.02.008
No abstract available
Keywords:
Brugada syndrome; MLPA; SCN5A; Ventricular fibrillation.
Publication types
Case Reports