Defects in early synaptic formation and neuronal function in Prader-Willi syndrome

Prader-Willi syndrome (PWS), which is a complex epigenetic disorder caused by the deficiency of paternally expressed genes in chromosome 15q11-q13, is associated with several psychiatric dimensions, including autism spectrum disorder. We have previously reported that iPS cells derived from PWS patie...

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Detalles Bibliográficos
Autores principales: Soeda, Shuhei, Ito, Daiki, Ogushi, Tomoe, Sano, Yui, Negoro, Ryosuke, Fujita, Takuya, Saito, Ryo, Taniura, Hideo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368700/
https://www.ncbi.nlm.nih.gov/pubmed/37491450
http://dx.doi.org/10.1038/s41598-023-39065-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368700/
https://www.ncbi.nlm.nih.gov/pubmed/37491450
http://dx.doi.org/10.1038/s41598-023-39065-x

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