Your browser doesn't support javascript.
loading
Expanding the phenotype of phosphomannomutase-2 gene congenital disorder of glycosylation: Cervical dystonia.
Rossi, Malco; Medina Escobar, Alex; Ameghino, Lucia; Merello, Marcelo.
Affiliation
  • Rossi M; Movement Disorders Section, Neuroscience Department, Raul Carrea Institute for Neurological Research (FLENI), Buenos Aires, Argentina.
  • Medina Escobar A; Movement Disorders Section, Neuroscience Department, Raul Carrea Institute for Neurological Research (FLENI), Buenos Aires, Argentina.
  • Ameghino L; Movement Disorders Section, Neuroscience Department, Raul Carrea Institute for Neurological Research (FLENI), Buenos Aires, Argentina.
  • Merello M; Movement Disorders Section, Neuroscience Department, Raul Carrea Institute for Neurological Research (FLENI), Buenos Aires, Argentina; Argentine National Scientific and Technological Research Council (CONICET), Argentina. Electronic address: mmerello@fleni.org.ar.
J Neurol Sci ; 378: 52-54, 2017 07 15.
Article in En | MEDLINE | ID: mdl-28566178

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Torticollis / Phosphotransferases (Phosphomutases) / Congenital Disorders of Glycosylation Type of study: Diagnostic_studies Limits: Adult / Female / Humans Language: En Journal: J Neurol Sci Year: 2017 Document type: Article Affiliation country: Argentina

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Torticollis / Phosphotransferases (Phosphomutases) / Congenital Disorders of Glycosylation Type of study: Diagnostic_studies Limits: Adult / Female / Humans Language: En Journal: J Neurol Sci Year: 2017 Document type: Article Affiliation country: Argentina
...