ABSTRACT
Mutations in genes encoding nuclear lamins cause diseases called laminopathies. In this issue, Hasper et al. (https//doi.org/10.1083/jcb.202307049) show that lamin A/C and the prelamin A variant in Hutchinson-Gilford progeria syndrome have relatively long lifetimes in affected tissues.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Progéria
/
Lamina Tipo A
Idioma:
En
Ano de publicação:
2024
Tipo de documento:
Article