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Reactivation of autophagy ameliorates LMNA cardiomyopathy
Mutations in the LMNA gene, which encodes lamin A and C (lamin A/C), cause a diverse spectrum of tissue-selective diseases termed laminopathies. The most prevalent form affects striated muscles as dilated cardiomyopathy with variable skeletal muscle involvement, which includes autosomal Emery-Dreifu...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Landes Bioscience
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3542212/ https://ncbi.nlm.nih.gov/pubmed/23044536 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/auto.22403 |
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