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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2008
Pynciau:
Article
Mynediad Ar-lein: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
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg