When Lamins Go Bad: Nuclear Structure and Disease: Cell
Progeria: old before their time - ScienceDirect
Progeria: A Paradigm for Translational Medicine: Cell
Speeding up the clock: The past, present and future of progeria - Swahari - 2016 - Development, Growth & Differentiation - Wiley Online Library
Progeria - Wikipedia
Base editor repairs mutation found in the premature-ageing syndrome progeria
Progeria
Cureus | Hutchinson-Gilford Progeria Syndrome: A Literature Review | Article
Children living with progeria - MedCrave online
Progeria (Hutchinson-Gilford Progeria Syndrome — HGPS): Symptoms & Causes
Progerin - Wikipedia
Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental Disomy
Progeria - About the Disease - Genetic and Rare Diseases Information Center
Base editor repairs mutation found in the premature-ageing syndrome progeria
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics
Life According To Sam Berns | MedPage Today
Pharmacotherapy to gene editing: potential therapeutic approaches for Hutchinson–Gilford progeria syndrome | SpringerLink
Hutchinson-Gilford Progeria Syndrome | IntechOpen
From the Rarest to the Most Common: Insights from Progeroid Syndromes into Skin Cancer and Aging - ScienceDirect
Hutchinson Gilford Progeria syndrome is caused by a single base change... | Download Scientific Diagram
Lamin A Truncation in Hutchinson-Gilford Progeria | Science
Hutchinson-Gilford progeria syndrome: MedlinePlus Genetics
LMNA mutations in progeria patients. The diagram shows the structure of... | Download Scientific Diagram
CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics
David R. Liu on Twitter: "The mutation (discovered by @NIHDirector's lab in 2003) results in progerin, a toxic protein that damages nuclei. So providing more healthy LMNA is not a solution, and
LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome | Journal of Medical Genetics
