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Huntington disease
Nature Reviews Disease Primers volume 1, Article number: 15052 (2015)
Huntington disease is an autosomal dominant neurological disorder caused by mutation in HTT. As illustrated here, the disease typically manifests in adulthood and is characterized by progressive motor, cognitive and behavioural impairment.
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Huntington disease. Nat Rev Dis Primers 1, 15052 (2015). https://doi.org/10.1038/nrdp.2015.52
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DOI: https://doi.org/10.1038/nrdp.2015.52
