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Bringing light into the darkness: autosomal recessive cerebellar ataxia due to a recessive mutation in the SEPSECS gene.
Martínez-Martín, Á; García-García, J; Díaz-Maroto Cicuéndez, I; Quintanilla-Mata, M L; Segura, T.
Affiliation
  • Martínez-Martín Á; Servicio de Neurología, Complejo Hospitalario Universitario de Albacete, Albacete, Spain. Electronic address: alvaro.martnzmd@gmail.com.
  • García-García J; Servicio de Neurología, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
  • Díaz-Maroto Cicuéndez I; Servicio de Neurología, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
  • Quintanilla-Mata ML; Servicio de Genética, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
  • Segura T; Servicio de Neurología, Complejo Hospitalario Universitario de Albacete, Albacete, Spain.
Neurologia (Engl Ed) ; 37(8): 709-710, 2022 10.
Article in En | MEDLINE | ID: mdl-35637137
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebellar Ataxia / Heredity Limits: Humans Language: En Journal: Neurologia (Engl Ed) Year: 2022 Document type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebellar Ataxia / Heredity Limits: Humans Language: En Journal: Neurologia (Engl Ed) Year: 2022 Document type: Article