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Differential regulation of non-protein coding RNAs from Prader-Willi Syndrome locus
Prader-Willi Syndrome (PWS) is a neurogenetic disorder caused by the deletion of imprinted genes on the paternally inherited human chromosome 15q11-q13. This locus harbours a long non-protein-coding RNA (U-UBE3A-ATS) that contains six intron-encoded snoRNAs, including the SNORD116 and SNORD115 repet...
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| Auteurs principaux: | , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Nature Publishing Group
2014
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4171697/ https://ncbi.nlm.nih.gov/pubmed/25246219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep06445 |
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