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Clinical and molecular consequences of exon 78 deletion in DMD gene.
Traverso, Monica; Assereto, Stefania; Baratto, Serena; Iacomino, Michele; Pedemonte, Marina; Diana, Maria Cristina; Ferretti, Marta; Broda, Paolo; Minetti, Carlo; Gazzerro, Elisabetta; Madia, Francesca; Bruno, Claudio; Zara, Federico; Fiorillo, Chiara.
Afiliação
  • Traverso M; DINOGMI, University of Genoa, Genoa, Italy.
  • Assereto S; Paediatric Neurology and Muscular Diseases Unit, University of Genoa and G. Gaslini Institute, Genoa, Italy.
  • Baratto S; Paediatric Neurology and Muscular Diseases Unit, University of Genoa and G. Gaslini Institute, Genoa, Italy.
  • Iacomino M; DINOGMI, University of Genoa, Genoa, Italy.
  • Pedemonte M; Paediatric Neurology and Muscular Diseases Unit, University of Genoa and G. Gaslini Institute, Genoa, Italy.
  • Diana MC; Paediatric Neurology and Muscular Diseases Unit, University of Genoa and G. Gaslini Institute, Genoa, Italy.
  • Ferretti M; Paediatric Neurology and Muscular Diseases Unit, University of Genoa and G. Gaslini Institute, Genoa, Italy.
  • Broda P; Paediatric Neurology and Muscular Diseases Unit, University of Genoa and G. Gaslini Institute, Genoa, Italy.
  • Minetti C; DINOGMI, University of Genoa, Genoa, Italy.
  • Gazzerro E; Paediatric Neurology and Muscular Diseases Unit, University of Genoa and G. Gaslini Institute, Genoa, Italy.
  • Madia F; Paediatric Neurology and Muscular Diseases Unit, University of Genoa and G. Gaslini Institute, Genoa, Italy.
  • Bruno C; Laboratory of Neurogenetic and Neuroscience, G. Gaslini Institute, Genoa, Italy.
  • Zara F; Paediatric Neurology and Muscular Diseases Unit, University of Genoa and G. Gaslini Institute, Genoa, Italy.
  • Fiorillo C; Laboratory of Neurogenetic and Neuroscience, G. Gaslini Institute, Genoa, Italy.
J Hum Genet ; 63(6): 761-764, 2018 Jun.
Article em En | MEDLINE | ID: mdl-29556034
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Éxons / Distrofina / Deleção de Genes / Creatina Quinase / Distrofia Muscular de Duchenne Tipo de estudo: Prognostic_studies Limite: Adolescent / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Éxons / Distrofina / Deleção de Genes / Creatina Quinase / Distrofia Muscular de Duchenne Tipo de estudo: Prognostic_studies Limite: Adolescent / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article