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Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
Mutations in the lamin A/C gene (LMNA) cause a variety of human diseases including Emery-Dreifuss muscular dystrophy, dilated cardiomyopathy, and Hutchinson-Gilford progeria syndrome. The tissue-specific effects of lamin mutations are unclear, in part because the function of lamin A/C is incompletel...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Clinical Investigation
2004
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC324542/ https://ncbi.nlm.nih.gov/pubmed/14755334 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200419670 |
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