Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures

Dysregulation of transcriptional pathways is observed in multiple forms of neurodevelopmental disorders (NDDs), such as intellectual disability (ID), epilepsy and autism spectrum disorder (ASD). We previously demonstrated that the NDD genes encoding lysine-specific demethylase 5C (KDM5C) and its tra...

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Detalles Bibliográficos
Autores principales: Poeta, Loredana, Padula, Agnese, Lioi, Maria Brigida, van Bokhoven, Hans, Miano, Maria Giuseppina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305412/
https://www.ncbi.nlm.nih.gov/pubmed/34356104
http://dx.doi.org/10.3390/genes12071088

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305412/
https://www.ncbi.nlm.nih.gov/pubmed/34356104
http://dx.doi.org/10.3390/genes12071088

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