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β-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi

Spinocerebellar ataxia type 5 (SCA5) is an autosomal dominant neurodegenerative disorder caused by mutations in β-III spectrin. A mouse lacking full-length β-III spectrin has a phenotype closely mirroring symptoms of SCA5 patients. Here we report the analysis of heterozygous animals, which show no s...

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Detalhes bibliográficos
Main Authors: Clarkson, Yvonne L., Gillespie, Trudi, Perkins, Emma M., Lyndon, Alastair R., Jackson, Mandy
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2928133/
https://ncbi.nlm.nih.gov/pubmed/20603325
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq279
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