Associated Papers
NUS1 and Epilepsy-myoclonus-ataxia Syndrome: An Under-recognized Entity?
Riboldi GM et al.
Tremor and Other Hyperkinetic Movements (new York, N.y.), 2022
Case Report: Clinical Features of a Chinese Boy With Epileptic Seizures and Intellectual Disabilities Who Carries a Truncated NUS1 Variant.
Zhang P et al.
Frontiers in Pediatrics, 2021
Recurrent NUS1 canonical splice donor site mutation in two unrelated individuals with epilepsy, myoclonus, ataxia and scoliosis - a case report.
Den K et al.
Bmc Neurology, 2019
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