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Fayl:Hutchinson-Gilford Progeria Syndrome.png

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Taʼrif 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).
Sanasi Published: November 15, 2005
Manba 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
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joriy23:44, 2006-yil 4-dekabrMiniatyurasi yoʻq1 200 × 968 (1,09 MB)wikimediacommons>Ayacop{{Information |Description='''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

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