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Parkin (PARK 2) mutations are rare in Czech patients with early-onset Parkinson's disease.
Fiala, Ondrej; Zahorakova, Daniela; Pospisilova, Lenka; Kucerova, Jana; Matejckova, Milada; Martasek, Pavel; Roth, Jan; Ruzicka, Evzen.
Afiliación
  • Fiala O; Department of Neurology and Centre of Clinical Neuroscience, 1st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic; Institute of Neuropsychiatric Care (INEP), Prague, Czech Republic.
  • Zahorakova D; Department of Pediatrics and Adolescent Medicine, 1st Faculty of Medicine, and General University Hospital, Charles University, Prague, Czech Republic.
  • Pospisilova L; Department of Pediatrics and Adolescent Medicine, 1st Faculty of Medicine, and General University Hospital, Charles University, Prague, Czech Republic.
  • Kucerova J; Department of Pediatrics and Adolescent Medicine, 1st Faculty of Medicine, and General University Hospital, Charles University, Prague, Czech Republic.
  • Matejckova M; Department of Pathology and Molecular Medicine, Thomayer's University Hospital, Prague, Czech Republic.
  • Martasek P; Department of Pediatrics and Adolescent Medicine, 1st Faculty of Medicine, and General University Hospital, Charles University, Prague, Czech Republic.
  • Roth J; Department of Neurology and Centre of Clinical Neuroscience, 1st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic.
  • Ruzicka E; Department of Neurology and Centre of Clinical Neuroscience, 1st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic.
PLoS One ; 9(9): e107585, 2014.
Article en En | MEDLINE | ID: mdl-25238391

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Ubiquitina-Proteína Ligasas / Mutación Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: República Checa

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Ubiquitina-Proteína Ligasas / Mutación Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: República Checa