Promising therapeutic aspects in human genetic imprinting disorders

Genomic imprinting is an epigenetic phenomenon of monoallelic gene expression pattern depending on parental origin. In humans, congenital imprinting disruptions resulting from genetic or epigenetic mechanisms can cause a group of diseases known as genetic imprinting disorders (IDs). Genetic IDs invo...

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Detalles Bibliográficos
Autores principales: Chao, Yunqi, Qin, Yifang, Zou, Xinyi, Wang, Xiangzhi, Hu, Chenxi, Xia, Fangling, Zou, Chaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655922/
https://www.ncbi.nlm.nih.gov/pubmed/36371218
http://dx.doi.org/10.1186/s13148-022-01369-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655922/
https://www.ncbi.nlm.nih.gov/pubmed/36371218
http://dx.doi.org/10.1186/s13148-022-01369-6

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