Your browser doesn't support javascript.
loading
One­carbon metabolism factor MTHFR variant is associated with saccade latency in Spinocerebellar Ataxia type 2.
Almaguer-Mederos, Luis E; Jorge-Sainz, Yasnay; Almaguer-Gotay, Dennis; Aguilera-Rodríguez, Raúl; Rodríguez-Labrada, Roberto; Velázquez-Pérez, Luis; González-Zaldívar, Yanetza; Cuello-Almarales, Dany; Vázquez-Mojena, Yaimé; Canales-Ochoa, Nalia; Aguiar-Santiago, Jorge; Auburger, Georg; MacLeod, Patrick.
Afiliación
  • Almaguer-Mederos LE; Center for the Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín, Cuba; University of Medical Sciences of Holguín, Cuba. Electronic address: lalmaguermederos@gmail.com.
  • Jorge-Sainz Y; University of Medical Sciences of Holguín, Cuba.
  • Almaguer-Gotay D; Center for the Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín, Cuba; University of Medical Sciences of Holguín, Cuba.
  • Aguilera-Rodríguez R; Center for the Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín, Cuba; University of Medical Sciences of Holguín, Cuba.
  • Rodríguez-Labrada R; Center for the Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín, Cuba.
  • Velázquez-Pérez L; Center for the Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín, Cuba.
  • González-Zaldívar Y; Center for the Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín, Cuba; University of Medical Sciences of Holguín, Cuba.
  • Cuello-Almarales D; Center for the Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín, Cuba; University of Medical Sciences of Holguín, Cuba.
  • Vázquez-Mojena Y; Center for the Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín, Cuba.
  • Canales-Ochoa N; Center for the Investigation and Rehabilitation of Hereditary Ataxias (CIRAH), Holguín, Cuba.
  • Aguiar-Santiago J; Center of Genetic Engineering and Biotechnology (CIGB), La Habana, Cuba.
  • Auburger G; Experimental Neurology, Goethe University Medical School, Frankfurt 60590, Germany.
  • MacLeod P; Division of Medical Genetics, Department of Pathology, Laboratory Medicine and Medical Genetics, Victoria General Hospital, Canada.
J Neurol Sci ; 409: 116586, 2020 Feb 15.
Article en En | MEDLINE | ID: mdl-31812845
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Movimientos Sacádicos / Variación Genética / Ataxias Espinocerebelosas / Polimorfismo de Nucleótido Simple / Metilenotetrahidrofolato Reductasa (NADPH2) Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurol Sci Año: 2020 Tipo del documento: Article Pais de publicación: Países Bajos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Movimientos Sacádicos / Variación Genética / Ataxias Espinocerebelosas / Polimorfismo de Nucleótido Simple / Metilenotetrahidrofolato Reductasa (NADPH2) Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurol Sci Año: 2020 Tipo del documento: Article Pais de publicación: Países Bajos