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Facial Hemiplegia Treated with Botulinum Toxin: A Case Report
In Prader–Willi syndrome (PWS), a genetic disorder characterized by mild-to-moderate ID, impaired behavior, and depression [118], paternal alleles of GABRA5 , GABRB3 , and GABRG3 are missing due to the partial deletion of an imprinted region on paternal chromosome 15 (15q11–13) [119]
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