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Specific contribution of lamin A and lamin C in the development of laminopathies
Mutations in the lamin A/C gene are involved in multiple human disorders for which the pathophysiological mechanisms are partially understood. Conflicting results prevail regarding the organization of lamin A and C mutants within the nuclear envelope (NE) and on the interactions of each lamin to its...
Tallennettuna:
| Päätekijät: | , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2008
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3934841/ https://ncbi.nlm.nih.gov/pubmed/18538321 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yexcr.2008.04.017 |
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