Hutchinson-Gilford_Progeria_Syndrome.png
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Description Hutchinson-Gilford Progeria Syndrome.png | Hutchinson-Gilford Progeria Syndrome. HGPS is a childhood disorder caused by mutations in one of the major architectural proteins of the cell nucleus. In HGPS patients the cell nucleus has dramatically aberrant morphology (bottom, right) rather than the uniform shape typically found in healthy individuals (top, right). | ||
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 doi:10.1371/journal.pbio.0030395 | ||
Author | See Source | ||
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