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Molecular ageing in progeroid syndromes: Hutchinson-Gilford progeria syndrome as a model
Hutchinson-Gilford progeria syndrome (HGPS) is a rare premature aging disorder that belongs to a group of conditions called laminopathies which affect nuclear lamins. Mutations in two genes, LMNA and ZMPSTE24, have been found in patients with HGPS. The p.G608G LMNA mutation is the most commonly repo...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2674425/ https://ncbi.nlm.nih.gov/pubmed/19379495 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1742-4933-6-4 |
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