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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 […]

IEC 2017 – Day 3 – Highlights

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Published Online: Sep 13th 2017

IEC 2017 Day 3 highlights from Barcelona.

View Day 1 highlights here.

View Day 2 highlights here.

View Day 4 highlights here.

Content produced and shared with kind authorisation of the International Epilepsy Congress (IEC 2017).

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