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Autor:
Leslie B. Gordon, Sammy Basso, Justine Maestranzi, Elena Aikawa, Cassandra L. Clift, Antonio Giovanni Cammardella, Tommaso Hinna Danesi, Pedro J. del Nido, Elazer R. Edelman, Abeer Hamdy, Sheila M. Hegde, Monica E. Kleinman, Nicola Maschietto, Mandeep R. Mehra, Srinivasan Mukundan, Francesco Musumeci, Marco Russo, Frank J. Rybicki, Pinak Bipin Shah, William A. Suarez, Kelsey Tuminelli, Katherine Zaleski, Ashwin Prakash, Marie Gerhard-Herman
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
Hutchinson-Gilford Progeria Syndrome (HGPS) is an ultra-rare genetic premature aging disease that is historically fatal in teenage years, secondary to severe accelerated atherosclerosis. The only approved treatment is the farnesyltransferase inhibito
Externí odkaz:
https://doaj.org/article/c233db4a024145d3811d09fb96c52220
