DNA methylation signatures in Blood DNA of Hutchinson–Gilford Progeria syndrome
<p dir="ltr">Hutchinson–Gilford Progeria Syndrome (HGPS) is an extremely rare genetic disorder caused by mutations in the <i>LMNA</i> gene and characterized by premature and accelerated aging beginning in childhood. In this study, we performed the first genome-wide methyl...
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| Main Author: | Yosra Bejaoui (8552574) (author) |
|---|---|
| Other Authors: | Aleem Razzaq (14779189) (author), Noha A. Yousri (1392577) (author), Junko Oshima (1626) (author), Andre Megarbane (3485465) (author), Abeer Qannan (14779192) (author), Ramya Potabattula (4401160) (author), Tanvir Alam (638619) (author), George M. Martin (14779195) (author), Henning F. Horn (14152938) (author), Thomas Haaf (342924) (author), Steve Horvath (28847) (author), Nady El Hajj (686554) (author) |
| Published: |
2022
|
| Subjects: | |
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