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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...
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| Vydáno v: | F1000Res |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
F1000Research
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5635448/ https://ncbi.nlm.nih.gov/pubmed/29093808 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.11610.1 |
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