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5. Eyelid myoclonia with absences, intellectual disability and attention deficit hyperactivity disorder: a clinical phenotype of the RORB gene mutation. Morea A, Boero G, Demaio V, Francavilla T, La Neve A. Neurol Sci; 2021 May; 42(5):2059-2062. PubMed ID: 33387058 [Abstract] [Full Text] [Related]
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