| Details |
| Disease Name | Prader-Willi Syndrome |
| Nocoding RNA Name | SNORD116 |
| Expression Pattern | differentially expressed |
| Species | Homo sapiens |
| Detection Methods | microarray etc. |
| Target | N/A |
| Tissue | blood |
| Treatment | N/A |
| PubMed ID | 24311433 |
| Year | 2014 |
| Detail Description | Our case adds further information about genotype–phenotype correlation and supports the hypothesis that SNORD116 plays a major role in the pathogenesis of Prader-Willi syndrome. |
NSDNA: The Nervous System Disease NcRNAome Atlas
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