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Huntington's Disease (HD): Neurodegeneration of Brodmann's Primary Visual Area 17 (BA17)
Huntington's disease (HD), an autosomal dominantly inherited polyglutamine or CAG repeat disease along with somatomotor, oculomotor, psychiatric and cognitive symptoms, presents clinically with impairments of elementary and complex visual functions as well as altered visual‐evoked potentials (V...
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| Publicado en: | Brain Pathol |
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| Autores principales: | , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2015
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8029049/ https://ncbi.nlm.nih.gov/pubmed/25495445 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bpa.12237 |
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