Epigenetic disorders: Lessons from the animals–animal models in chromatinopathies

Chromatinopathies are defined as genetic disorders caused by mutations in genes coding for protein involved in the chromatin state balance. So far 82 human conditions have been described belonging to this group of congenital disorders, sharing some molecular features and clinical signs. For almost a...

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Detalles Bibliográficos
Autores principales: Di Fede, Elisabetta, Grazioli, Paolo, Lettieri, Antonella, Parodi, Chiara, Castiglioni, Silvia, Taci, Esi, Colombo, Elisa Adele, Ancona, Silvia, Priori, Alberto, Gervasini, Cristina, Massa, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548571/
https://www.ncbi.nlm.nih.gov/pubmed/36225316
http://dx.doi.org/10.3389/fcell.2022.979512

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548571/
https://www.ncbi.nlm.nih.gov/pubmed/36225316
http://dx.doi.org/10.3389/fcell.2022.979512

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