Identifying key underlying regulatory networks and predicting targets of orphan C/D box SNORD116 snoRNAs in Prader-Willi syndrome

Prader-Willi syndrome (PWS) is a rare neurodevelopmental disorder characterized principally by initial symptoms of neonatal hypotonia and failure-to-thrive in infancy, followed by hyperphagia and obesity. It is well established that PWS is caused by loss of paternal expression of the imprinted regio...

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Detalles Bibliográficos
Autores principales: Gilmore, Rachel B., Liu, Yaling, Stoddard, Christopher E., Chung, Michael S., Carmichael, Gordon G., Cotney, Justin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592975/
https://www.ncbi.nlm.nih.gov/pubmed/37873184
http://dx.doi.org/10.1101/2023.10.03.560773

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592975/
https://www.ncbi.nlm.nih.gov/pubmed/37873184
http://dx.doi.org/10.1101/2023.10.03.560773

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