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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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| Pubblicato in: | Hum Brain Mapp |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2015
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| Soggetti: | |
| Accesso online: | 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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