Your browser doesn't support javascript.
loading
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype.
Ghezzi, Andrea; Martinelli, Ilaria; Carra, Serena; Mediani, Laura; Zucchi, Elisabetta; Simonini, Cecilia; Gianferrari, Giulia; Fini, Nicola; Cereda, Cristina; Gellera, Cinzia; Pensato, Viviana; Mandrioli, Jessica.
Afiliação
  • Ghezzi A; Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Martinelli I; Clinical and Experimental Medicine PhD Program, University of Modena and Reggio Emilia, Modena, Italy. martinelli.ilaria88@gmail.com.
  • Carra S; Department of Neurosciences, Azienda Ospedaliero-Universitaria Di Modena, Modena, Italy. martinelli.ilaria88@gmail.com.
  • Mediani L; Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Zucchi E; Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Simonini C; Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Gianferrari G; Department of Neurosciences, Azienda Ospedaliero-Universitaria Di Modena, Modena, Italy.
  • Fini N; Department of Neurosciences, Azienda Ospedaliero-Universitaria Di Modena, Modena, Italy.
  • Cereda C; Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Gellera C; Department of Neurosciences, Azienda Ospedaliero-Universitaria Di Modena, Modena, Italy.
  • Pensato V; Genomic and Post-Genomic Unit IRCCS - Mondino Foundation, Pavia, Italy.
  • Mandrioli J; Unit of Medical Genetics and Neurogenetics - Fondazione, IRCCS Istituto Neurologico 'Carlo Besta', Milan, Italy.
Neurol Sci ; 43(10): 6087-6090, 2022 Oct.
Article em En | MEDLINE | ID: mdl-35731316
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Neurol Sci Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Neurol Sci Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália