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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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| 發表在: | Hum Brain Mapp |
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| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley and Sons Inc.
2015
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| 主題: | |
| 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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