Reference Genes across Nine Brain Areas of Wild Type and Prader-Willi Syndrome Mice: Assessing Differences in Igfbp7, Pcsk1, Nhlh2 and Nlgn3 Expression

Prader–Willi syndrome (PWS) is a complex neurodevelopmental disorder caused by the deletion or inactivation of paternally expressed imprinted genes at the chromosomal region 15q11–q13. The PWS-critical region (PWScr) harbors tandemly repeated non-protein coding IPW-A exons hosting the intronic SNORD...

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Detalles Bibliográficos
Autores principales: Kummerfeld, Delf-Magnus, Skryabin, Boris V., Brosius, Juergen, Vakhrushev, Sergey Y., Rozhdestvensky, Timofey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369261/
https://www.ncbi.nlm.nih.gov/pubmed/35955861
http://dx.doi.org/10.3390/ijms23158729

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369261/
https://www.ncbi.nlm.nih.gov/pubmed/35955861
http://dx.doi.org/10.3390/ijms23158729

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