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An Association Study of DNA Methylation and Gene Expression in Angelman Syndrome: A Bioinformatics Approach

Angelman syndrome (AS) is a neurodevelopmental disorder caused by the loss of function of the E3-ligase UBE3A. Despite multiple studies, AS pathophysiology is still obscure and has mostly been explored in rodent models of the disease. In recent years, a growing body of studies has utilized omics dat...

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Detalles Bibliográficos
Autores principales: Panov, Julia, Kaphzan, Hanoch
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9409443/
https://www.ncbi.nlm.nih.gov/pubmed/36012404
http://dx.doi.org/10.3390/ijms23169139

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