Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene

Bibliographic Details
Main Authors: Anders Krogh Broendberg, MD, Lisbeth Noerum Pedersen, MSc, PhD, Jens Cosedis Nielsen, MD, DMSc, PhD, Henrik Kjaerulf Jensen, MD, DMSc, PhD
Format: Article
Language:English
Published: Elsevier 2016-05-01
Series:HeartRhythm Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2214027116300161
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spelling doaj-9d6c5ba322e347c298ee7dc900f267f02021-07-02T01:48:16ZengElsevierHeartRhythm Case Reports2214-02712016-05-012326126410.1016/j.hrcr.2016.02.008Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A geneAnders Krogh Broendberg, MD0Lisbeth Noerum Pedersen, MSc, PhD1Jens Cosedis Nielsen, MD, DMSc, PhD2Henrik Kjaerulf Jensen, MD, DMSc, PhD3Department of Cardiology, Aarhus University Hospital, Aarhus, DenmarkDepartment of Molecular Medicine, Aarhus University Hospital, Aarhus, DenmarkDepartment of Cardiology, Aarhus University Hospital, Aarhus, DenmarkDepartment of Cardiology, Aarhus University Hospital, Aarhus, Denmarkhttp://www.sciencedirect.com/science/article/pii/S2214027116300161Brugada syndromeMLPASCN5AVentricular fibrillation
collection DOAJ
language English
format Article
sources DOAJ
author Anders Krogh Broendberg, MD
Lisbeth Noerum Pedersen, MSc, PhD
Jens Cosedis Nielsen, MD, DMSc, PhD
Henrik Kjaerulf Jensen, MD, DMSc, PhD
spellingShingle Anders Krogh Broendberg, MD
Lisbeth Noerum Pedersen, MSc, PhD
Jens Cosedis Nielsen, MD, DMSc, PhD
Henrik Kjaerulf Jensen, MD, DMSc, PhD
Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
HeartRhythm Case Reports
Brugada syndrome
MLPA
SCN5A
Ventricular fibrillation
author_facet Anders Krogh Broendberg, MD
Lisbeth Noerum Pedersen, MSc, PhD
Jens Cosedis Nielsen, MD, DMSc, PhD
Henrik Kjaerulf Jensen, MD, DMSc, PhD
author_sort Anders Krogh Broendberg, MD
title Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
title_short Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
title_full Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
title_fullStr Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
title_full_unstemmed Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
title_sort repeated molecular genetic analysis in brugada syndrome revealed a novel disease-associated large deletion in the scn5a gene
publisher Elsevier
series HeartRhythm Case Reports
issn 2214-0271
publishDate 2016-05-01
topic Brugada syndrome
MLPA
SCN5A
Ventricular fibrillation
url http://www.sciencedirect.com/science/article/pii/S2214027116300161
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