Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide

In this part of a series on founder mutations in the Netherlands, we review a Dutch family carrying the SCN5a 1795insD mutation. We describe the advances in our understanding of the premature sudden cardiac deaths that have accompanied this family in the past centuries. The mutation carriers show a...

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Detalhes bibliográficos
Main Authors: Postema, P.G., Van den Berg, M., Van Tintelen, J.P., Van den Heuvel, F., Grundeken, M., Hofman, N., Van der Roest, W.P., Nannenberg, E.A., Krapels, I.P.C., Bezzina, C.R., Wilde, A.
Formato: Artigo
Idioma:Inglês
Publicado em: Bohn Stafleu van Loghum 2009
Assuntos:
Review Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2779479/
https://ncbi.nlm.nih.gov/pubmed/19949711
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