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

Autor:	Lisbeth Noerum Pedersen, Anders Krogh Broendberg, Jens Cosedis Nielsen, Henrik Jensen
Rok vydání:	2016
Předmět:	0301 basic medicine medicine.medical_specialty Scn5a gene Case Report Disease 030204 cardiovascular system & hematology Bioinformatics 03 medical and health sciences 0302 clinical medicine Internal medicine medicine Diseases of the circulatory (Cardiovascular) system Brugada syndrome Ventricular fibrillation Multiplex ligation-dependent probe amplification SCN5A business.industry medicine.disease MLPA Molecular analysis 030104 developmental biology RC666-701 Cardiology Cardiology and Cardiovascular Medicine business
Zdroj:	HeartRhythm Case Reports, Vol 2, Iss 3, Pp 261-264 (2016) Krogh Brøndberg, A, Pedersen, L N, Nielsen, J C & Jensen, H K 2016, ' Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene ', HeartRhythm Case Reports, vol. 2, no. 3, pp. 261-264 . https://doi.org/10.1016/j.hrcr.2016.02.008 HeartRhythm Case Reports
ISSN:	2214-0271
DOI:	10.1016/j.hrcr.2016.02.008
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2df869e7e466e6b41fb6ad0bad564355 https://doi.org/10.1016/j.hrcr.2016.02.008 Zobrazit plný text záznamu