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Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case report

scholarly article by Kathrin Nickel et al published 2 August 2018 in BMC Psychiatry

New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel CACNA1C Loss-Of-Function Mutation

artículo científico publicado en 2020

Schizophrenia and Hereditary Polyneuropathy: Deletion as a Common Pathophysiological Link?

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