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Merideth MA., Gordon LB., Clauss S., Sachdev V., Smith AC., Perry MB., Brewer CC., Zalewski C., Kim HJ., Solomon B., Brooks BP., Gerber LH., Turner ML., Domingo DL., Hart TC., Graf J., Reynolds JC., Gropman A., Yanovski JA., Gerhard-Herman M., Collins FS., Nabel EG., Cannon RO., Gahl WA., Introne WJ. Phenotype and course of Hutchinson-Gilford progeria syndrome. „The New England journal of medicine”. 6 (358), s. 592–604, luty 2008. DOI: 10.1056/NEJMoa0706898. PMID: 18256394.
McClintock D., Ratner D., Lokuge M., Owens DM., Gordon LB., Collins FS., Djabali K. The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin. „PLoS ONE”. 12 (2), s. e1269, 2007. DOI: 10.1371/journal.pone.0001269. PMID: 18060063.
Korf B. Hutchinson-Gilford progeria syndrome, aging, and the nuclear lamina. „The New England journal of medicine”. 6 (358), s. 552–555, luty 2008. DOI: 10.1056/NEJMp0800071. PMID: 18256390.