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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 […]

Glutamate Dysregulation Involved in Pediatric Bipolar Disorder

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Published Online: Dec 31st 2014

Andrea Spencer, M.D., speaks with Psychiatric News about the association of glutamatergic dysregulation in pediatric bipolar disorder.

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