Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene
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Elsevier
2016-05-01
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Series: | HeartRhythm Case Reports |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S2214027116300161 |
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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 |
work_keys_str_mv |
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1721344301204504576 |