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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2010
Aiheet:
Articles
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia