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A truncated lamin A in the Lmna(−/−) mouse line: Implications for the understanding of laminopathies
During recent years a number of severe clinical syndromes, collectively termed laminopathies, turned out to be caused by various, distinct mutations in the human LMNA gene. Arising from this, remarkable progress has been made to unravel the molecular pathophysiology underlying these disorders. A gre...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Landes Bioscience
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3474667/ https://ncbi.nlm.nih.gov/pubmed/22895093 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/nucl.21676 |
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