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Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications
Next-generation sequencing (NGS) is now more accessible to clinicians and researchers. As a result, our understanding of the genetics of neurodevelopmental disorders (NDDs) has rapidly advanced over the past few years. NGS has led to the discovery of new NDD genes with an excess of recurrent de novo...
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| Udgivet i: | Genome Med |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5704398/ https://ncbi.nlm.nih.gov/pubmed/29179772 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-017-0498-x |
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