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Study reveals connection between brain protein, movement disorder in children

Researchers have shed light on the molecular events that underpin an inherited movement and neurodegenerative disorder known as ARSACS - Autosomal recessive spastic ataxia of Charlevoix-Saguenay, named after two Quebec valleys where the first cases were discovered.

Scientists Reveal Role of Key Brain Protein in Childhood Movement Disorder

Scientists Reveal Role of Key Brain Protein in Childhood Movement Disorder
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Scientists illuminate the molecular events underlying childhood movement disorder

Scientists at the UNC School of Medicine and UNC Eshelman School of Pharmacy, in collaboration with a team from Queen Mary University of London, have illuminated the molecular events underlying an inherited movement and neurodegenerative disorder known as ARSACS – Autosomal recessive spastic ataxia of Charlevoix-Saguenay, named for two Quebec valleys where the first cases were found.

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