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==Hutchinson-Gilford Progeria Syndrome== | ==Hutchinson-Gilford Progeria Syndrome== | ||
:Links: [[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 | |||
:'''Links:''' [[Hutchinson-Gilford Progeria Syndrome]] | |||
===Reference=== | |||
[http://biology.plosjournals.org/perlserv/?request=get-document&doi=10.1371/journal.pbio.0030395 PLoS - The Cell Nucleus and Aging] | |||
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Revision as of 09:40, 15 March 2016
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 26) 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
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