File:Hutchinson-Gilford Progeria Syndrome.jpg

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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 lamin A

Image: PLoS - The Cell Nucleus and Aging

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current11:12, 16 March 2009Thumbnail for version as of 11:12, 16 March 2009600 × 484 (48 KB)S8600021 (talk | contribs)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 architect
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