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Translational Pathology Shared Resource Core Archives

Discovery sheds new light on Angelman, Prader-Willi syndromes

Dec. 22, 2016—A mutation associated with epilepsy and autism also is responsible for a “pale eye” trait in two rare genetic disorders, Angelman syndrome and Prader-Willi syndrome, neuroscientists at Vanderbilt University Medical Center reported this week.

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