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Sanger sequencing as a first-line approach for molecular diagnosis of Andersen-Tawil syndrome
In 1977, Frederick Sanger developed a new method for DNA sequencing based on the chain termination method, now known as the Sanger sequencing method (SSM). Recently, massive parallel sequencing, better known as next-generation sequencing (NGS), is replacing the SSM for detecting mutations in cardi...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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F1000Research
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635448/ https://www.ncbi.nlm.nih.gov/pubmed/29093808 http://dx.doi.org/10.12688/f1000research.11610.1 |