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Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging
Most cases of the segmental progeroid syndrome, Hutchinson–Gilford progeria syndrome (HGPS), are caused by a de novo dominant mutation within a single codon of the LMNA gene. This mutation leads to the increased usage of an internal splice site that generates an alternative lamin A transcript with a...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2986496/ https://ncbi.nlm.nih.gov/pubmed/19172989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2008.270 |
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