Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands

In this part of a series on cardiogenetic founder mutations in the Netherlands, we review the Dutch founder mutations in hypertrophic cardiomyopathy (HCM) patients. HCM is a common autosomal dominant genetic disease affecting at least one in 500 persons in the general population. Worldwide, most mut...

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Detalhes bibliográficos
Main Authors: Christiaans, I., Nannenberg, E.A., Dooijes, D., Jongbloed, R.J.E., Michels, M., Postema, P.G., Majoor-Krakauer, D., van den Wijngaard, A., Mannens, M.M.A.M., van Tintelen, J.P., van Langen, I.M., Wilde, A.A.M.
Formato: Artigo
Idioma:Inglês
Publicado em: Bohn Stafleu van Loghum 2010
Assuntos:
Review Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2871745/
https://ncbi.nlm.nih.gov/pubmed/20505798
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