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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Detalles Bibliográficos
Autores principales: MacLeod, Heather M, Culley, Mary R, Huber, Jill M, McNally, Elizabeth M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC169171/
https://www.ncbi.nlm.nih.gov/pubmed/12854972
http://dx.doi.org/10.1186/1471-2350-4-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC169171/
https://www.ncbi.nlm.nih.gov/pubmed/12854972
http://dx.doi.org/10.1186/1471-2350-4-4

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