F09 The study on molecular changes related to energy metabolism in Huntington's disease subjects: looking for biomarkers

Huntington's disease (HD) is a neurodegenerative disorder characterised by a progressive motor and cognitive decline and psychiatric symptoms. The origin of molecular and biochemical disturbances in HD is the genetic defect in the HTT gene, autosomally dominantly inherited. The altered huntingt...

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Veröffentlicht in:Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A23-A24
Hauptverfasser: Krzysztoń-Russjan, J, Zielonka, D, Jackiewicz, J, Kuśmirek, S, Bubko, I, Klimberg, A, Marcinkowski, JT, Anuszewska, EL
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Sprache:eng
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