Your browser doesn't support javascript.
loading
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient].
Klivényi, Péter; Szpisjak, László; Salamon, András; Németh, Viola Luca; Szépfalusi, Noémi; Maróti, Zoltán; Kalmár, Tibor; Zimmermann, Aliz; Zádori, Dénes.
Afiliación
  • Klivényi P; University of Szeged, Department of Neurology, Szeged.
  • Szpisjak L; University of Szeged, Department of Neurology, Szeged.
  • Salamon A; University of Szeged, Department of Neurology, Szeged.
  • Németh VL; University of Szeged, Department of Neurology, Szeged.
  • Szépfalusi N; University of Szeged, Department of Neurology, Szeged.
  • Maróti Z; University of Szeged, Genetic Diagnostic Laboratory, Department of Pediatrics and Pediatric Health Center, Szeged.
  • Kalmár T; University of Szeged, Genetic Diagnostic Laboratory, Department of Pediatrics and Pediatric Health Center, Szeged.
  • Zimmermann A; University of Szeged, Department of Pediatrics and Pediatric Health Center, Szeged.
  • Zádori D; University of Szeged, Department of Neurology, Szeged.
Ideggyogy Sz ; 76(1-2): 63-72, 2023 01 30.
Article en En | MEDLINE | ID: mdl-36892293
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Encefalopatías / Disartria Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies País/Región como asunto: Europa Idioma: En Revista: Ideggyogy Sz Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Encefalopatías / Disartria Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies País/Región como asunto: Europa Idioma: En Revista: Ideggyogy Sz Año: 2023 Tipo del documento: Article