A (GCC) repeat in SBF1 reveals a novel biological phenomenon in human and links to late onset neurocognitive disorder

The human SBF1 (SET binding factor 1) gene, alternatively known as MTMR5, is predominantly expressed in the brain, and its epigenetic dysregulation is linked to late-onset neurocognitive disorders (NCDs), such as Alzheimer’s disease. This gene contains a (GCC)-repeat at the interval between + 1 and ...

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Detalles Bibliográficos
Autores principales: Khamse, Safoura, Alizadeh, Samira, Bernhart, Stephan H., Afshar, Hossein, Delbari, Ahmad, Ohadi, Mina
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/PMC9474449/
https://www.ncbi.nlm.nih.gov/pubmed/36104480
http://dx.doi.org/10.1038/s41598-022-19878-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474449/
https://www.ncbi.nlm.nih.gov/pubmed/36104480
http://dx.doi.org/10.1038/s41598-022-19878-y

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