The progeria research foundation 10(th) international scientific workshop; researching possibilities, ExTENding lives – webinar version scientific summary

Progeria is an ultra-rare (prevalence 1 in 20 million), fatal, pediatric autosomal dominant premature aging disease caused by a mutation in the LMNA gene. This mutation results in accumulation of a high level of an aberrant form of the nuclear membrane protein, Lamin A. This aberrant protein, termed...

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Detalles Bibliográficos
Autores principales: Gordon, Leslie B., Tuminelli, Kelsey, Andrés, Vicente, Campisi, Judith, Kieran, Mark W., Doucette, Lynn, Gordon, Audrey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034973/
https://www.ncbi.nlm.nih.gov/pubmed/33735109
http://dx.doi.org/10.18632/aging.202835

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034973/
https://www.ncbi.nlm.nih.gov/pubmed/33735109
http://dx.doi.org/10.18632/aging.202835

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