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

Detalles Bibliográficos
Autores principales: Broendberg, Anders Krogh, Pedersen, Lisbeth Noerum, Nielsen, Jens Cosedis, Jensen, Henrik Kjaerulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419769/
https://www.ncbi.nlm.nih.gov/pubmed/28491684
http://dx.doi.org/10.1016/j.hrcr.2016.02.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419769/
https://www.ncbi.nlm.nih.gov/pubmed/28491684
http://dx.doi.org/10.1016/j.hrcr.2016.02.008

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