TY  - GEN 
AU  - Fafian Labora, Juan
AU  - Morente López, Miriam
AU  - De Toro Santos, Francisco Javier
AU  - Arufe Gonda, Mª del Carmen
PY  - 2021
SN  - 1661-6596
UR  - http://hdl.handle.net/20.500.11940/17394
AB  - Hutchinson-Gilford progeria syndrome (HGPS) is a deadly childhood disorder, which is considered a very rare disease. It is caused by an autosomal dominant mutation on the LMNA gene, and it is characterized by accelerated aging. Human cell lines from...
LA  - en
TI  - High-Throughput Screen Detects Calcium Signaling Dysfunction in Hutchinson-Gilford Progeria Syndrome
DO  - 10.3390/ijms22147327
VL  - 22
ER  -