Your browser doesn't support javascript.
loading
Correspondence on "Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment" by Roux et al.
Park, Joohyun; Deininger, Natalie; Rautenberg, Maren; Saft, Carsten; Harmuth, Florian; Sturm, Marc; Riess, Olaf; Schöls, Ludger; Synofzik, Matthis; Haack, Tobias B.
Afiliação
  • Park J; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. joohyun.park@med.uni-tuebingen.de.
  • Deininger N; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Rautenberg M; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Saft C; Department of Neurology, Huntington Centre NRW, Ruhr-University Bochum, St. Josef-Hospital, Bochum, Germany.
  • Harmuth F; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Sturm M; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Riess O; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Schöls L; Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.
  • Synofzik M; Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.
  • Haack TB; Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
Genet Med ; 23(6): 1171-1172, 2021 06.
Article em En | MEDLINE | ID: mdl-33564152

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia Cerebelar / Disfunção Cognitiva / Doenças do Sistema Nervoso Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia Cerebelar / Disfunção Cognitiva / Doenças do Sistema Nervoso Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article