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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 […]

FYI: New Therapeutic Strategies in Progressive Neuromuscular Disorders such as ALS

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Published Online: Nov 21st 2012

An educational series from Duke Clinical Research Institute, presented by Richard Bedlack, MD, PhD, MS

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