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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التفاصيل البيبلوغرافية
المؤلف الرئيسي:	Yosra Bejaoui (8552574) (author)
مؤلفون آخرون:	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)
منشور في:	2022
الموضوعات:	Biological sciences Biochemistry and cell biology Genetics Biomedical and clinical sciences Clinical sciences accelerated aging DNA methylation epigenetic clock Hutchinson–Gilford Progeria syndrome progeroid laminopathies
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!

DNA methylation signatures in Blood DNA of Hutchinson–Gilford Progeria syndrome

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