Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome

BACKGROUND AND OBJECTIVE: The long-QT syndrome (LQTS) is associated with premature sudden cardiac deaths affecting whole families and is caused by mutations in genes encoding for cardiac proteins. When the same mutation is found in different families (recurrent mutations), this may imply either a co...

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Detalles Bibliográficos
Autores principales: Hofman, N., Jongbloed, R., Postema, P. G., Nannenberg, E., Alders, M., Wilde, A. A. M.
Formato: Texto
Lenguaje:English
Publicado: Bohn Stafleu van Loghum 2010
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021187/
https://www.ncbi.nlm.nih.gov/pubmed/21350584
http://dx.doi.org/10.1007/s12471-010-0046-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021187/
https://www.ncbi.nlm.nih.gov/pubmed/21350584
http://dx.doi.org/10.1007/s12471-010-0046-4

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