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Autor:
Elisabetta Di Fede, Paolo Grazioli, Antonella Lettieri, Chiara Parodi, Silvia Castiglioni, Esi Taci, Elisa Adele Colombo, Silvia Ancona, Alberto Priori, Cristina Gervasini, Valentina Massa
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
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 m
Externí odkaz:
https://doaj.org/article/3af2ab1890a64ab4a7716bf6a4b9b466