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Basal ganglia‐cortical structural connectivity in Huntington's disease

Huntington's disease is an incurable neurodegenerative disease caused by inheritance of an expanded cytosine‐adenine‐guanine (CAG) trinucleotide repeat within the Huntingtin gene. Extensive volume loss and altered diffusion metrics in the basal ganglia, cortex and white matter are seen when pat...

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書目詳細資料
發表在:Hum Brain Mapp
Main Authors: Novak, Marianne J.U., Seunarine, Kiran K., Gibbard, Clare R., McColgan, Peter, Draganski, Bogdan, Friston, Karl, Clark, Chris A., Tabrizi, Sarah J.
格式: Artigo
語言:Inglês
出版: John Wiley and Sons Inc. 2015
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6869797/
https://ncbi.nlm.nih.gov/pubmed/25640796
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hbm.22733
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