Current scenario of the genetic testing for rare neurological disorders exploiting next generation sequencing

Next generation sequencing is currently a cornerstone of genetic testing in routine diagnostics, allowing for the detection of sequence variants with so far unprecedented large scale, mainly in genetically heterogenous diseases, such as neurological disorders. It is a fast-moving field, where new we...

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Detalles Bibliográficos
Autores principales: Di Resta, Chiara, Pipitone, Giovanni Battista, Carrera, Paola, Ferrari, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996035/
https://www.ncbi.nlm.nih.gov/pubmed/32985468
http://dx.doi.org/10.4103/1673-5374.293135

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996035/
https://www.ncbi.nlm.nih.gov/pubmed/32985468
http://dx.doi.org/10.4103/1673-5374.293135

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