Genomic instability and DNA replication defects in progeroid syndromes

Progeroid syndromes induced by mutations in lamin A or in its interactors – named progeroid laminopathies – are model systems for the dissection of the molecular pathways causing physiological and premature aging. A large amount of data, based mainly on the Hutchinson Gilford Progeria syndrome (HGPS...

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Bibliografiske detaljer
Udgivet i:Nucleus
Main Authors: Burla, Romina, La Torre, Mattia, Merigliano, Chiara, Vernì, Fiammetta, Saggio, Isabella
Format: Artigo
Sprog:Inglês
Udgivet: Taylor & Francis 2018
Fag:
Special Issue on Laminopathies
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7000143/
https://ncbi.nlm.nih.gov/pubmed/29936894
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19491034.2018.1476793
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