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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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| Foilsithe in: | Hum Mol Genet |
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| Main Authors: | , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Oxford University Press
2015
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| Ábhair: | |
| Rochtain Ar Líne: | 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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