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Molecular insights into the premature aging disease progeria
Hutchinson–Gilford progeria syndrome (HGPS) is an extremely rare premature aging disease presenting many features resembling the normal aging process. HGPS patients die before the age of 20 years due to cardiovascular problems and heart failure. HGPS is linked to mutations in the LMNA gene encoding...
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| Publicat a: | Histochem Cell Biol |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Berlin Heidelberg
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4796323/ https://ncbi.nlm.nih.gov/pubmed/26847180 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00418-016-1411-1 |
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