Your browser doesn't support javascript.
loading
A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 Gene.
Vinagre-Aragón, Ana; Campo-Caballero, David; Mondragón-Rezola, Elisabet; Pardina-Vilella, Lara; Hernandez Eguiazu, Haizea; Gorostidi, Ana; Croitoru, Ioana; Bergareche, Alberto; Ruiz-Martinez, Javier.
Affiliation
  • Vinagre-Aragón A; Department of Neurology, Hospital Universitario Donostia, San Sebastián, Spain.
  • Campo-Caballero D; Neuroscience Area, Biodonostia Health Research Institute, San Sebastián, Spain.
  • Mondragón-Rezola E; Department of Neurology, Hospital Universitario Donostia, San Sebastián, Spain.
  • Pardina-Vilella L; Neuroscience Area, Biodonostia Health Research Institute, San Sebastián, Spain.
  • Hernandez Eguiazu H; Department of Neurology, Hospital Universitario Donostia, San Sebastián, Spain.
  • Gorostidi A; Neuroscience Area, Biodonostia Health Research Institute, San Sebastián, Spain.
  • Croitoru I; Department of Neurology, Hospital Universitario Donostia, San Sebastián, Spain.
  • Bergareche A; Neuroscience Area, Biodonostia Health Research Institute, San Sebastián, Spain.
  • Ruiz-Martinez J; Neuroscience Area, Biodonostia Health Research Institute, San Sebastián, Spain.
Front Neurol ; 12: 635396, 2021.
Article in En | MEDLINE | ID: mdl-33763016

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Front Neurol Year: 2021 Document type: Article Affiliation country: Spain Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Front Neurol Year: 2021 Document type: Article Affiliation country: Spain Country of publication: Switzerland