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Charcot-Marie-Tooth disease due to MORC2 mutations in Spain.
Sivera, Rafael; Lupo, Vincenzo; Frasquet, Marina; Argente-Escrig, Herminia; Alonso-Pérez, Jorge; Díaz-Manera, Jordi; Querol, Luis; Del Mar García-Romero, María; Ignacio Pascual, Samuel; García-Sobrino, Tania; Paradas, Carmen; Francisco Vázquez-Costa, Juan; Muelas, Nuria; Millet, Elvira; Jesús Vílchez, Juan; Espinós, Carmen; Sevilla, Teresa.
Affiliation
  • Sivera R; Department of Neurology, Hospital Francesc de Borja, Gandía, Spain.
  • Lupo V; Unit of Rare Neurodegenerative Diseases Felipe, Centro de Investigación Príncipe, Valencia, Spain.
  • Frasquet M; Neuromuscular Diseases Unit, Department of Neurology, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
  • Argente-Escrig H; Neuromuscular and Ataxias Research Group, Instituto de Investigación Sanitaria La Fe, Valencia, Spain.
  • Alonso-Pérez J; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
  • Díaz-Manera J; Neuromuscular Diseases Unit, Department of Neurology, Hospital Universitari i Politècnic La Fe, Valencia, Spain.
  • Querol L; Neuromuscular and Ataxias Research Group, Instituto de Investigación Sanitaria La Fe, Valencia, Spain.
  • Del Mar García-Romero M; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
  • Ignacio Pascual S; Neuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • García-Sobrino T; Universitat Autonoma de Barcelona, Barcelona, Spain.
  • Paradas C; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
  • Francisco Vázquez-Costa J; Neuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Muelas N; Universitat Autonoma de Barcelona, Barcelona, Spain.
  • Millet E; John Walton Muscular Dystrophy Research Center, Newcastle University Translational and Clinical Research Institute, Newcastle Upon Tyne, UK.
  • Jesús Vílchez J; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
  • Espinós C; Neuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Sevilla T; Universitat Autonoma de Barcelona, Barcelona, Spain.
Eur J Neurol ; 28(9): 3001-3011, 2021 09.
Article in En | MEDLINE | ID: mdl-34189813

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease Type of study: Observational_studies / Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2021 Document type: Article Affiliation country: España Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease Type of study: Observational_studies / Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2021 Document type: Article Affiliation country: España Country of publication: Reino Unido