TY  - JOUR
AU  - Macicior Michelena, Jon
AU  - Marcos Ramiro, Beatriz
AU  - Ortega Gutiérrez, Silvia
PY  - 2021
DO  - 10.3390/ ijms22137190
SN  - 1422-0067
UR  - https://hdl.handle.net/20.500.14352/7471
T2  - International Journal of Molecular Sciences
AB  - Hutchinson–Gilford progeria syndrome (HGPS), or progeria, is an extremely rare disorder that belongs to the class of laminopathies, diseases characterized by alterations in the genes that encode for the lamin proteins or for their associated...
LA  - eng
PB  - MDPI
KW  - rare diseases
KW  - Hutchinson–Gilford progeria syndrome (HGPS)
KW  - progeria
KW  - progerin
KW  - lamin A
TI  - Small-Molecule Therapeutic Perspectives for the Treatment of Progeria
TY  - journal article
VL  - 22
ER  -