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MicroRNAs in hereditary and sporadic premature aging syndromes and other laminopathies
Hereditary and sporadic laminopathies are caused by mutations in genes encoding lamins, their partners, or the metalloprotease ZMPSTE24/FACE1. Depending on the clinical phenotype, they are classified as tissue‐specific or systemic diseases. The latter mostly manifest with several accelerated aging f...
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| Publicat a: | Aging Cell |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6052405/ https://ncbi.nlm.nih.gov/pubmed/29696758 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/acel.12766 |
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