Small-Molecule Therapeutic Perspectives for the Treatment of Progeria

Hutchinson–Gilford progeria syndrome (HGPS), or progeria, is an extremely rare disorder that belongs to the class of laminopathies, diseases characterized by alterations in the genes that encode for the lamin proteins or for their associated interacting proteins. In particular, progeria is caused by...

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Detalles Bibliográficos
Autores principales: Macicior, Jon, Marcos-Ramiro, Beatriz, Ortega-Gutiérrez, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267806/
https://www.ncbi.nlm.nih.gov/pubmed/34281245
http://dx.doi.org/10.3390/ijms22137190

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267806/
https://www.ncbi.nlm.nih.gov/pubmed/34281245
http://dx.doi.org/10.3390/ijms22137190

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