TY  - JOUR
AU  - Macías, Álvaro
AU  - Nevado, Rosa M
AU  - González-Gómez, Cristina
AU  - Gonzalo, Pilar
AU  - Andres-Manzano, Maria J.
AU  - Dorado, Beatriz
AU  - Benedicto, Ignacio
AU  - Andres, Vicente
PY  - 2023
DO  - 10.1007/s11357-023-00808-3
UR  - http://hdl.handle.net/20.500.12105/16218
AB  - Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic disease caused by expression of progerin, a lamin A variant that is also expressed at low levels in non-HGPS individuals. Although HGPS patients die predominantly from myocardial...
LA  - eng
PB  - Springer
TI  - Coronary and carotid artery dysfunction and KV7 overexpression in a mouse model of Hutchinson-Gilford progeria syndrome.
TY  - journal article
ER  -