Huntington disease (HD) is an autosomal dominant disorder with full penetrance and rare de novo mutations. Early changes include mild motor decline with clumsiness and slowed gait, progressive changes include dystonia and chorea, parkinsonian symptoms, slow and stiff...
CITATION STYLE
Weis, S., Sonnberger, M., Dunzinger, A., Voglmayr, E., Aichholzer, M., Kleiser, R., & Strasser, P. (2019). Neurodegenerative Diseases: Huntington Disease. In Imaging Brain Diseases (pp. 1059–1068). Springer Vienna. https://doi.org/10.1007/978-3-7091-1544-2_40
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