Base editor repairs mutation found in the premature-ageing syndrome progeria
Hutchinson-Gilford progeria patient-derived cardiomyocyte model of carrying LMNA gene variant c.1824 C > T,Cell and Tissue Research - X-MOL
Lamin A Truncation in Hutchinson-Gilford Progeria | Science
Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome | Journal of Medical Genetics
CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
Progeria: A Paradigm for Translational Medicine: Cell
Progeria: A Paradigm for Translational Medicine: Cell
The genetic mechanism that links Hutchinson-Gilford progeria syndrome to physiological aging. | Semantic Scholar
Gene Positioning
Speeding up the clock: The past, present and future of progeria - Swahari - 2016 - Development, Growth & Differentiation - Wiley Online Library
The Disorder That Makes One Age 7 Times Faster | Hutchinson-Gilford Progeria Syndrome and its Recent Advances | Science Repository | Open Access Journals