Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis

Prader-Willi syndrome (PWS) is a rare neurodevelopmental disorder caused by a loss of usually paternally expressed, maternally imprinted genes located on chromosome 15q11-q13. Individuals with PWS display a specific behavioral phenotype and have a higher susceptibility than the general population fo...

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Detalles Bibliográficos
Autores principales: Heseding, Hannah M., Jahn, Kirsten, Eberlein, Christian K., Wieting, Jelte, Maier, Hannah B., Proskynitopoulos, Phileas J., Glahn, Alexander, Bleich, Stefan, Frieling, Helge, Deest, Maximilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187685/
https://www.ncbi.nlm.nih.gov/pubmed/35688807
http://dx.doi.org/10.1038/s41398-022-02014-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187685/
https://www.ncbi.nlm.nih.gov/pubmed/35688807
http://dx.doi.org/10.1038/s41398-022-02014-9

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