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Lamin A/C truncation in dilated cardiomyopathy with conduction disease
BACKGROUND: Mutations in the gene encoding the nuclear membrane protein lamin A/C have been associated with at least 7 distinct diseases including autosomal dominant dilated cardiomyopathy with conduction system disease, autosomal dominant and recessive Emery Dreifuss Muscular Dystrophy, limb girdle...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2003
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC169171/ https://ncbi.nlm.nih.gov/pubmed/12854972 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-4-4 |
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