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Joseph Samaha, Jim Dagher, Shayan Abdollah Zadegan

Huntington’s disease (HD) is a neurodegenerative disease inherited in an autosomal dominant manner. It is caused by an expansion of cytosine, adenine, guanine (CAG) repeats within the huntingtin (HTT) gene, which is located on chromosome 4. This pathological expansion of CAG repeats results in the production of a mutant huntingtin protein with an abnormally long polyglutamine […]

ESOC 2016 – Day 1 – Highlights

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Published Online: May 11th 2016

Highlights from the first day of the 2nd European Stroke Organisation Conference (ESOC 2016)


Content produced and shared with the kind authorisation of the European Stroke Organisation (ESO)

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