Your browser doesn't support javascript.
loading
A New Homozygous CACNB2 Mutation has Functional Relevance and Supports a Role for Calcium Channels in Autism Spectrum Disorder.
Graziano, Claudio; Despang, Patrick; Palombo, Flavia; Severi, Giulia; Posar, Annio; Cassio, Alessandra; Pippucci, Tommaso; Isidori, Federica; Matthes, Jan; Bonora, Elena.
Afiliação
  • Graziano C; Unit of Medical Genetics, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138, Bologna, Italy. claudio.graziano@unibo.it.
  • Despang P; Department of Pharmacology, University of Cologne, Cologne, Germany.
  • Palombo F; IRCCS Istituto Delle Scienze Neurologiche Di Bologna, UOC Clinica Neurologica, Bologna, Italy.
  • Severi G; Unit of Medical Genetics, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138, Bologna, Italy.
  • Posar A; IRCCS Istituto Delle Scienze Neurologiche Di Bologna, UOC Neuropsichiatria Infantile, Bologna, Italy.
  • Cassio A; Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
  • Pippucci T; Unit of Pediatrics, S. Orsola-Malpighi Hospital, Bologna, Italy.
  • Isidori F; Unit of Medical Genetics, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138, Bologna, Italy.
  • Matthes J; Unit of Medical Genetics, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138, Bologna, Italy.
  • Bonora E; Department of Pharmacology, University of Cologne, Cologne, Germany.
J Autism Dev Disord ; 51(1): 377-381, 2021 01.
Article em En | MEDLINE | ID: mdl-32506348
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Autism Dev Disord Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Autism Dev Disord Ano de publicação: 2021 Tipo de documento: Article