Your browser doesn't support javascript.
loading
FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees.
Brenner, David; Müller, Kathrin; Lattante, Serena; Yilmaz, Rüstem; Knehr, Antje; Freischmidt, Axel; Ludolph, Albert C; Andersen, Peter M; Weishaupt, Jochen H.
  • Brenner D; Division of Neurodegeneration, Department of Neurology, Mannheim Center for Translational Neurosciences (MCTN), Medical Faculty Mannheim, Heidelberg University, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany.
  • Müller K; Department of Neurology, University of Ulm, Ulm, Germany.
  • Lattante S; Section of Genomic Medicine, Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Yilmaz R; Unit of Medical Genetics, Department of Laboratory and Infectious Disease Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Knehr A; Division of Neurodegeneration, Department of Neurology, Mannheim Center for Translational Neurosciences (MCTN), Medical Faculty Mannheim, Heidelberg University, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany.
  • Freischmidt A; Division of Neurodegeneration, Department of Neurology, Mannheim Center for Translational Neurosciences (MCTN), Medical Faculty Mannheim, Heidelberg University, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Germany.
  • Ludolph AC; Department of Neurology, University of Ulm, Ulm, Germany.
  • Andersen PM; Department of Neurology, University of Ulm, Ulm, Germany.
  • Weishaupt JH; Department of Neurology, University of Ulm, Ulm, Germany.
Neurogenetics ; 23(1): 59-65, 2022 01.
Article en En | MEDLINE | ID: mdl-34518945
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Demencia Frontotemporal / Esclerosis Amiotrófica Lateral Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Demencia Frontotemporal / Esclerosis Amiotrófica Lateral Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article