Laddar...
Loss of the imprinted, non-coding Snord116 gene cluster in the interval deleted in the Prader Willi syndrome results in murine neuronal and endocrine pancreatic developmental phenotypes
Global neurodevelopmental delay is a prominent characteristic of individuals with Prader-Willi syndrome (PWS). The neuromolecular bases for these delays are unknown. We identified neuroanatomical changes in the brains of mice deficient for a gene in the minimal critical deletion region for PWS (Snor...
Sparad:
| I publikationen: | Hum Mol Genet |
|---|---|
| Huvudupphovsmän: | , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2017
|
| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5815655/ https://ncbi.nlm.nih.gov/pubmed/28973544 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx342 |
| Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|