Molecular subtyping and improved treatment of neurodevelopmental disease

The next-generation sequencing revolution has substantially increased our understanding of the mutated genes that underlie complex neurodevelopmental disease. Exome sequencing has enabled us to estimate the number of genes involved in the etiology of neurodevelopmental disease, whereas targeted sequ...

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Detalles Bibliográficos
Autores principales: Stessman, Holly A. F., Turner, Tychele N., Eichler, Evan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Opinion
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766622/
https://www.ncbi.nlm.nih.gov/pubmed/26917491
http://dx.doi.org/10.1186/s13073-016-0278-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766622/
https://www.ncbi.nlm.nih.gov/pubmed/26917491
http://dx.doi.org/10.1186/s13073-016-0278-z

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