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Specific contribution of lamin A and lamin C in the development of laminopathies

Mutations in the lamin A/C gene are involved in multiple human disorders for which the pathophysiological mechanisms are partially understood. Conflicting results prevail regarding the organization of lamin A and C mutants within the nuclear envelope (NE) and on the interactions of each lamin to its...

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Detalhes bibliográficos
Main Authors: Sylvius, Nicolas, Hathaway, Andrea, Boudreau, Emilie, Gupta, Pallavi, Labib, Sarah, Bolongo, Pierrette M., Rippstein, Peter, McBride, Heidi, Bilinska, Zofia T., Tesson, Frédérique
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3934841/
https://ncbi.nlm.nih.gov/pubmed/18538321
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yexcr.2008.04.017
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