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.
Authors
Claudio Graziano
1
,
Patrick Despang
2
,
Flavia Palombo
3
,
Giulia Severi
4
,
Annio Posar
5
6
,
Alessandra Cassio
7
,
Tommaso Pippucci
4
,
Federica Isidori
4
,
Jan Matthes
2
,
Elena Bonora
8
Affiliations
1
Unit of Medical Genetics, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138, Bologna, Italy.
[email protected]
.
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.
[email protected]
.
PMID:
32506348
DOI:
10.1007/s10803-020-04551-y
No abstract available
Publication types
Letter
Grants and funding
GGP15171/Fondazione Telethon