SNORD116 and growth hormone therapy impact IGFBP7 in Prader–Willi syndrome

PURPOSE: Prader–Willi syndrome (PWS) is a neurodevelopmental disorder with hypothalamic dysfunction due to deficiency of imprinted genes located on the 15q11-q13 chromosome. Among them, the SNORD116 gene appears critical for the expression of the PWS phenotype. We aimed to clarify the role of SNORD1...

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Detalles Bibliográficos
Autores principales: Eddiry, Sanaa, Diene, Gwenaelle, Molinas, Catherine, Salles, Juliette, Auriol, Françoise Conte, Gennero, Isabelle, Bieth, Eric, Skryabin, Boris V., Rozhdestvensky, Timofey S., Burnett, Lisa C., Leibel, Rudolph L., Tauber, Maithé, Salles, Jean Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460435/
https://www.ncbi.nlm.nih.gov/pubmed/34040195
http://dx.doi.org/10.1038/s41436-021-01185-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460435/
https://www.ncbi.nlm.nih.gov/pubmed/34040195
http://dx.doi.org/10.1038/s41436-021-01185-y

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