High prevalence of genetic variants previously associated with LQT syndrome in new exome data

To date, hundreds of variants in 13 genes have been associated with long QT syndrome (LQTS). The prevalence of LQTS is estimated to be between 1:2000 and 1:5000. The knowledge of genetic variation in the general population has until recently been limited, but newly published data from NHLBI GO Exome...

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Detalles Bibliográficos
Main Authors: Refsgaard, Lena, Holst, Anders G, Sadjadieh, Golnaz, Haunsø, Stig, Nielsen, Jonas B, Olesen, Morten S
Formato: Artigo
Idioma:Inglês
Publicado: Nature Publishing Group 2012
Assuntos:
Short Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3400735/
https://ncbi.nlm.nih.gov/pubmed/22378279
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.23
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