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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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Detalhes bibliográficos
Publicado no:Genes (Basel)
Main Authors: Poeta, Loredana, Padula, Agnese, Lioi, Maria Brigida, van Bokhoven, Hans, Miano, Maria Giuseppina
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8305412/
https://ncbi.nlm.nih.gov/pubmed/34356104
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12071088
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