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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 […]

Neuromuscular Diseases

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Published Online: Jul 22nd 2014

Specialists at Georgia Regents Neuroscience Center of Excellence diagnose and treat neuromuscular disorders that affect muscle control, pain, weakness, or spasticity.

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