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Exome sequencing in a child with neurodevelopmental disorder and epilepsy: Variant analysis of the AHNAK2 gene.
Vinci, Mirella; Kursula, Petri; Greco, Donatella; Elia, Maurizio; Vetri, Luigi; Schepis, Carmelo; Chiavetta, Valeria; Donadio, Serena; Roccella, Michele; Carotenuto, Marco; Romano, Valentino; Calì, Francesco.
Afiliação
  • Vinci M; Oasi Research Institute-IRCCS, Troina, Italy.
  • Kursula P; Department of Biomedicine, University of Bergen, Bergen, Norway.
  • Greco D; Biocenter Oulu & Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.
  • Elia M; Oasi Research Institute-IRCCS, Troina, Italy.
  • Vetri L; Oasi Research Institute-IRCCS, Troina, Italy.
  • Schepis C; Oasi Research Institute-IRCCS, Troina, Italy.
  • Chiavetta V; Oasi Research Institute-IRCCS, Troina, Italy.
  • Donadio S; Oasi Research Institute-IRCCS, Troina, Italy.
  • Roccella M; Department of Sciences for Health Promotion and Mother and Child Care "G. D'Alessandro", University of Palermo, Palermo, Italy.
  • Carotenuto M; Department of Psychology, Educational Science and Human Movement, University of Palermo, Palermo, Italy.
  • Romano V; Clinic of Child and Adolescent Neuropsychiatry, Department of Mental Health, Physical and Preventive Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
  • Calì F; Department of Biological, Chemical and Pharmaceutical Sciences and Technologies, University of Palermo, Palermo, Italy.
Mol Genet Genomic Med ; 10(9): e2012, 2022 09.
Article em En | MEDLINE | ID: mdl-35789128
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia / Transtornos do Neurodesenvolvimento Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia / Transtornos do Neurodesenvolvimento Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2022 Tipo de documento: Article