Neurodevelopmental disorder with dystonia due to SOX6 mutations
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DOI: 10.1002/mgg3.2051
Abstract: Mutations in SOX6 have recently been recognized as a new molecular cause of neurodevelopmental disorders characterized by intellectual disability, behavioral changes, and nonspecific facial and digital skeletal abnormalities. To date, read more here.
Keywords: neurodevelopmental disorder; dystonia due; due sox6; disorder dystonia ... See more keywords