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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 […]

EAN 2017 – Joaquim Ferreira Interview – Part 1

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Published Online: Jul 12th 2017

EAN Programme Committee Member, Prof. Joaquim Ferreira, talks about the most significant recent developments with respect to movement disorders and what he considers will be the most exciting/promising developments over the next 2 years. Part 1 of 2.

View Part 2 here.

Speaker disclosures: nothing to disclose in relation to this video interview.

Filmed at the 3rd Congress of the European Academy of Neurology (EAN), Amsterdam, June 2017.

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