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Identification of long non-coding RNAs involved in neuronal development and intellectual disability
Recently, exome sequencing led to the identification of causal mutations in 16–31% of patients with intellectual disability (ID), leaving the underlying cause for many patients unidentified. In this context, the noncoding part of the human genome remains largely unexplored. For many long non-coding...
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| I publikationen: | Sci Rep |
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| Huvudupphovsmän: | , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Nature Publishing Group
2016
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4913242/ https://ncbi.nlm.nih.gov/pubmed/27319317 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep28396 |
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