File:Hutchinson-Gilford Progeria Syndrome.jpg
From Embryology
No higher resolution available.
Hutchinson-Gilford_Progeria_Syndrome.jpg (600 × 484 pixels, file size: 48 KB, MIME type: image/jpeg)
Hutchinson-Gilford Progeria Syndrome
In more than 80% of cases the gene defect responsible for HGPS is a single spontaneous mutation in codon 608 of the LMNA gene, which encodes both lamin A and lamin C
- progerin is a mutant form of the nuclear architectural protein lamina A
Reference
PLoS - The Cell Nucleus and Aging
Cite this page: Hill, M.A. (2024, June 17) Embryology Hutchinson-Gilford Progeria Syndrome.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Hutchinson-Gilford_Progeria_Syndrome.jpg
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
File history
Yi efo/eka'e gwa ebo wo le nyangagi wuncin ye kamina wunga tinya nan
| Gwalagizhi | Nyangagi | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 09:39, 15 March 2016 | | 600 × 484 (48 KB) | Z8600021 (talk | contribs) | ==Hutchinson-Gilford Progeria Syndrome== :Links: Hutchinson-Gilford Progeria Syndrome |
You cannot overwrite this file.
File usage
The following page uses this file:
