TY  - GEN
AU  - Benedicto, Ignacio
AU  - Hamczyk, Magda R
AU  - Nevado, Rosa M
AU  - Barettino, Ana
AU  - Carmona, Rosa M
AU  - Espinós-Estévez, Carla
AU  - Gonzalo, Pilar
AU  - de la Fuente-Pérez, Miguel
AU  - Andrés-Manzano, María J
AU  - González-Gómez, Cristina
AU  - Dorado, Beatriz
AU  - Andrés, Vicente
PY  - 2024
UR  - https://hdl.handle.net/20.500.12105/25841
AB  - Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disorder caused by a mutation in the LMNA gene that provokes the synthesis of progerin, a mutant version of the nuclear protein lamin A that accelerates aging and precipitates death. The...
LA  - eng
PB  - Wiley
KW  - Hutchinson‐Gilford progeria syndrome
KW  - atherosclerosis
KW  - cardiovascular disease
KW  - endothelial cells
KW  - progerin
TI  - Endothelial cell-specific progerin expression does not cause cardiovascular alterations and premature death.
TY  - research article
ER  -