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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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| Опубликовано в: : | Hum Brain Mapp |
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| Главные авторы: | , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
John Wiley and Sons Inc.
2015
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| Предметы: | |
| Online-ссылка: | 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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