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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...
| Autores principales: | , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Bohn Stafleu van Loghum
2010
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| Materias: | |
| 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 |