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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Impact Journals
2021
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| 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 |