An ovine transgenic Huntington's disease model

Huntington's disease (HD) is an inherited autosomal dominant neurodegenerative disorder caused by an expansion of a CAG trinucleotide repeat in the huntingtin (HTT) gene [Huntington's Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expande...

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Detalhes bibliográficos
Main Authors: Jacobsen, Jessie C., Bawden, C. Simon, Rudiger, Skye R., McLaughlan, Clive J., Reid, Suzanne J., Waldvogel, Henry J., MacDonald, Marcy E., Gusella, James F., Walker, Simon K., Kelly, Jennifer M., Webb, Graham C., Faull, Richard L.M., Rees, Mark I., Snell, Russell G.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2860888/
https://ncbi.nlm.nih.gov/pubmed/20154343
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq063
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