| Details |
| Disease Name | Prader-Willi Syndrome |
| Nocoding RNA Name | IPW |
| Expression Pattern | up-regulated |
| Species | Homo sapiens |
| Detection Methods | qRT-PCR etc. |
| Target | N/A |
| Tissue | cell lines(fibroblast cell lines) |
| Treatment | N/A |
| PubMed ID | 24816254 |
| Year | 2014 |
| Detail Description | Our results suggest that a subset of PWS phenotypes may arise from dysregulation of an imprinted locus distinct from the PWS region. |
NSDNA: The Nervous System Disease NcRNAome Atlas
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