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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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| Gepubliceerd in: | Genome Med |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2016
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4766622/ https://ncbi.nlm.nih.gov/pubmed/26917491 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-016-0278-z |
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