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Disruption of the lamin A and matrin-3 interaction by myopathic LMNA mutations
The nuclear face of the nuclear membrane is enriched with the intermediate filament protein lamin A. Mutations in LMNA, the gene encoding lamin A, lead to a diverse set of inherited conditions including myopathies that affect both the heart and skeletal muscle. To gain insight about lamin A protein...
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| Vydáno v: | Hum Mol Genet |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4492393/ https://ncbi.nlm.nih.gov/pubmed/25948554 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv160 |
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