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Screening of Therapeutic Strategies for Huntington's Disease in YAC128 Transgenic Mice

Huntington's disease (HD) is a hereditary neurodegenerative disorder caused by an unstable expansion of cytosine‐adenine‐guanine (CAG) repeats in the HD gene. The symptoms include cognitive dysfunction and severe motor impairment with loss of voluntary movement coordination that is later replac...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:CNS Neurosci Ther
Päätekijä: Gil‐Mohapel, Joana M.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Blackwell Publishing Ltd 2011
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6493426/
https://ncbi.nlm.nih.gov/pubmed/21501423
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1755-5949.2011.00246.x
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