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Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesis.
Brackmann, Florian; Coras, Roland; Rössler, Karl; Kraus, Cornelia; Rompel, Oliver; Trollmann, Regina.
Afiliación
  • Brackmann F; Department of Pediatrics, Neuropediatrics, Friedrich-Alexander University of Erlangen-Nürnberg, Erlangen, Germany. Electronic address: florian.brackmann@uk-erlangen.de.
  • Coras R; Department of Neuropathology, Friedrich-Alexander University of Erlangen-Nürnberg, Erlangen, Germany.
  • Rössler K; Department of Neurosurgery, Friedrich-Alexander University of Erlangen-Nürnberg, Erlangen, Germany.
  • Kraus C; Department of Human Genetics, Friedrich-Alexander University of Erlangen-Nürnberg, Erlangen, Germany.
  • Rompel O; Department of Radiology, Friedrich-Alexander University of Erlangen-Nürnberg, Erlangen, Germany.
  • Trollmann R; Department of Pediatrics, Neuropediatrics, Friedrich-Alexander University of Erlangen-Nürnberg, Erlangen, Germany.
Brain Dev ; 40(4): 330-333, 2018 Apr.
Article en En | MEDLINE | ID: mdl-29191363
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paraparesia / Enfermedad de Alexander / Proteína Ácida Fibrilar de la Glía / Mutación Tipo de estudio: Diagnostic_studies Idioma: En Revista: Brain Dev Año: 2018 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Paraparesia / Enfermedad de Alexander / Proteína Ácida Fibrilar de la Glía / Mutación Tipo de estudio: Diagnostic_studies Idioma: En Revista: Brain Dev Año: 2018 Tipo del documento: Article