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Letter to the Editor Regarding the Article "Whole-Exome Sequencing in NF1-Related West's Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy".
Vetri, Luigi; Calì, Francesco; Vinci, Mirella; Amato, Carmelo; Roccella, Michele; Granata, Tiziana; Freri, Elena; Solazzi, Roberta; Romano, Valentino; Elia, Maurizio.
Afiliação
  • Vetri L; Oasi Research Institute-IRCCS, Troina, Italy.
  • Calì F; Department of Sciences for Health Promotion and Mother and Child Care "G. D'Alessandro" University of Palermo, Palermo, Italy.
  • Vinci M; Oasi Research Institute-IRCCS, Troina, Italy.
  • Amato C; Department of Sciences for Health Promotion and Mother and Child Care "G. D'Alessandro" University of Palermo, Palermo, Italy.
  • Roccella M; Oasi Research Institute-IRCCS, Troina, Italy.
  • Granata T; Department of Psychology, Educational Science and Human Movement, University of Palermo, Palermo, Italy.
  • Freri E; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Solazzi R; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Romano V; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Elia M; Department of Biological, Chemical and Pharmaceutical Sciences and Technologies, University of Palermo, Palermo, Italy.
Neuropediatrics ; 52(2): 153, 2021 04.
Article em En | MEDLINE | ID: mdl-33111300
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Epilepsia Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Epilepsia Idioma: En Ano de publicação: 2021 Tipo de documento: Article