The Imprinted NPAP1 Gene in the Prader–Willi Syndrome Region Belongs to a POM121-Related Family of Retrogenes

We have recently shown that the human Nuclear pore-associated protein (NPAP1)/C15orf2 gene encodes a nuclear pore-associated protein. This gene is one of several paternally expressed imprinted genes in the genomic region 15q11q13. Because the Prader–Willi syndrome is known to be caused by the loss o...

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Detalles Bibliográficos
Autores principales: Neumann, Lisa C., Feiner, Nathalie, Meyer, Axel, Buiting, Karin, Horsthemke, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942032/
https://www.ncbi.nlm.nih.gov/pubmed/24482533
http://dx.doi.org/10.1093/gbe/evu019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942032/
https://www.ncbi.nlm.nih.gov/pubmed/24482533
http://dx.doi.org/10.1093/gbe/evu019

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