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Description Hutchinson-Gilford Progeria Syndrome. HGPS is a childhood disorder caused by mutations in one of the major architectural proteins of the cell nucleus.
Date Published: November 15, 2005
Source The Cell Nucleus and Aging: Tantalizing Clues and Hopeful Promises. Scaffidi P, Gordon L, Misteli T. PLoS Biology Vol. 3/11/2005, e395 https://dx.doi.org/10.1371/journal.pbio.0030395
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With image of aberrant cell nuclei.

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Date/TimeThumbnailDimensionsUserComment
current11:06, 17 May 2009Thumbnail for version as of 11:06, 17 May 2009354 × 484 (424 KB)Mikael Häggström{{Information |Description={{en|1=g}} |Source=g |Author=g |Date=g |Permission= |other_versions= }} <!--{{ImageUpload|full}}-->

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