An overview of treatment strategies for Hutchinson-Gilford Progeria syndrome

Hutchinson-Gilford progeria syndrome (HGPS) is a sporadic, autosomal dominant disorder characterized by premature and accelerated aging symptoms leading to death at the mean age of 14.6 years usually due to cardiovascular complications. HGPS is caused by a de novo point mutation in the LMNA gene enc...

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Detalles Bibliográficos
Autores principales: Harhouri, Karim, Frankel, Diane, Bartoli, Catherine, Roll, Patrice, De Sandre-Giovannoli, Annachiara, Lévy, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Laminopathies
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973194/
https://www.ncbi.nlm.nih.gov/pubmed/29619863
http://dx.doi.org/10.1080/19491034.2018.1460045

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