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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Detalles Bibliográficos
Autores principales: Totomoch-Serra, Armando, Marquez, Manlio F., Cervantes-Barragán, David E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Opinion Article
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

Internet

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

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