A New Homozygous CACNB2 Mutation has Functional Relevance and Supports a Role for Calcium Channels in Autism Spectrum Disorder

J Autism Dev Disord. 2021 Jan;51(1):377-381. doi: 10.1007/s10803-020-04551-y.

¹ Unit of Medical Genetics, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138, Bologna, Italy. claudio.graziano@unibo.it.
² Department of Pharmacology, University of Cologne, Cologne, Germany.
³ IRCCS Istituto Delle Scienze Neurologiche Di Bologna, UOC Clinica Neurologica, Bologna, Italy.
⁴ Unit of Medical Genetics, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138, Bologna, Italy.
⁵ IRCCS Istituto Delle Scienze Neurologiche Di Bologna, UOC Neuropsichiatria Infantile, Bologna, Italy.
⁶ Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
⁷ Unit of Pediatrics, S. Orsola-Malpighi Hospital, Bologna, Italy.
⁸ Unit of Medical Genetics, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138, Bologna, Italy. elena.bonora6@unibo.it.

No abstract available

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