TY  - GEN
AU  - Chen, Xue
AU  - Yao, Haidong
AU  - Andres, Vicente
AU  - Bergo, Martin O
AU  - Kashif, Muhammad
PY  - 2022
DO  - 10.1111/bcpt.13770
UR  - http://hdl.handle.net/20.500.12105/15912
AB  - Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disorder characterized by premature ageing and early death at a mean age of 14.7 years. At the molecular level, HGPS is caused by a de novo heterozygous mutation in LMNA, the gene encoding...
LA  - eng
PB  - Wiley
KW  - Progeria
KW  - Adolescent
KW  - Farnesyltranstransferase
KW  - Humans
KW  - Lamin Type A
KW  - Nuclear Proteins
KW  - Protein Processing, Post-Translational
TI  - Status of treatment strategies for Hutchinson-Gilford progeria syndrome with a focus on prelamin: A posttranslational modification.
TY  - review
ER  -