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A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrhea.
Bommarito, G; Cellerino, M; Prada, V; Venturi, C; Capellari, S; Cortelli, P; Mancardi, G L; Parchi, P; Schenone, A.
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  • Bommarito G; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa and Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
  • Cellerino M; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa and Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
  • Prada V; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa and Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
  • Venturi C; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa and Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
  • Capellari S; Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
  • Cortelli P; IRCCS Istituto delle Scienze Neurologiche, Bologna, Italy.
  • Mancardi GL; Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
  • Parchi P; IRCCS Istituto delle Scienze Neurologiche, Bologna, Italy.
  • Schenone A; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa and Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Eur J Neurol ; 25(8): e91-e92, 2018 08.
Article en En | MEDLINE | ID: mdl-29984897
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Italia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Italia