File:Hutchinson-Gilford Progeria Syndrome.png

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current18:44, 4 December 2006Thumbnail for version as of 18:44, 4 December 20061,200 × 968 (1.09 MB)commons>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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