Phenotype and Course of Hutchinson–Gilford Progeria Syndrome

BACKGROUND: Hutchinson–Gilford progeria syndrome is a rare, sporadic, autosomal dominant syndrome that involves premature aging, generally leading to death at approximately 13 years of age due to myocardial infarction or stroke. The genetic basis of most cases of this syndrome is a change from glyci...

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Päätekijät: Merideth, Melissa A., Gordon, Leslie B., Clauss, Sarah, Sachdev, Vandana, Smith, Ann C.M., Perry, Monique B., Brewer, Carmen C., Zalewski, Christopher, Kim, H. Jeffrey, Solomon, Beth, Brooks, Brian P., Gerber, Lynn H., Turner, Maria L., Domingo, Demetrio L., Hart, Thomas C., Graf, Jennifer, Reynolds, James C., Gropman, Andrea, Yanovski, Jack A., Gerhard-Herman, Marie, Collins, Francis S., Nabel, Elizabeth G., Cannon, Richard O., Gahl, William A., Introne, Wendy J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2008
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2940940/
https://ncbi.nlm.nih.gov/pubmed/18256394
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1056/NEJMoa0706898
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