Comprehensive Phenotype of the p.Arg420his Allelic Form of Spinocerebellar Ataxia Type 13

Overview of attention for article published in The Cerebellum, August 2013

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Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 gene

Article in BMC Neurology (June 2023)

Ion Channel Genes and Ataxia

Book chapter (May 2023)

Epilepsy as the Symptom of a Spinocerebellar Ataxia 13 in a Patient Presenting with a Mutation in the KCNC3 Gene

Preprint in Research Square (April 2023)