TY  - GEN
AU  - Benedicto, Ignacio
AU  - Hamczyk, Magda R
AU  - Dorado, Beatriz
AU  - Andrés, Vicente
PY  - 2026
DO  - 10.1016/j.molmed.2025.03.005
UR  - https://hdl.handle.net/20.500.12105/27754
AB  - Hutchinson-Gilford progeria syndrome (HGPS) is an ultrarare genetic disease caused by progerin, a broadly expressed mutant variant of lamin A protein that accelerates aging and leads to premature death typically in adolescence. Progerin affects many...
LA  - eng
KW  - Hutchinson-Gilford progeria syndrome
KW  - atherosclerosis
KW  - cardiovascular disease
KW  - endothelial cells
KW  - progerin
KW  - vascular smooth muscle cells
KW  - Humans
KW  - Animals
KW  - Lamin Type A
KW  - Atherosclerosis
TI  - Vascular cell types in progeria: victims or villains?
TY  - research article
ER  -