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

Hutchinson–Gilford Progeria Syndrome (HGPS) is an extremely rare genetic disorder caused by mutations in the LMNA gene and characterized by premature and accelerated aging beginning in childhood. In this study, we performed the first genome‐wide methylation analysis on blood DNA of 15 patients with...

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Detalles Bibliográficos
Autores principales: Bejaoui, Yosra, Razzaq, Aleem, Yousri, Noha A., Oshima, Junko, Megarbane, Andre, Qannan, Abeer, Potabattula, Ramya, Alam, Tanvir, Martin, George M., Horn, Henning F., Haaf, Thomas, Horvath, Steve, El Hajj, Nady
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844112/
https://www.ncbi.nlm.nih.gov/pubmed/35045206
http://dx.doi.org/10.1111/acel.13555

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844112/
https://www.ncbi.nlm.nih.gov/pubmed/35045206
http://dx.doi.org/10.1111/acel.13555

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