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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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| Autores principales: | , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Nature Publishing Group
2012
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| Materias: | |
| Acceso en línea: | 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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