LMNB1 mutation causes cerebellar involvement and a genome instability defect

  • J Neurol Sci. 2017 Aug 15;379:249-252. doi: 10.1016/j.jns.2017.06.027.
José Luiz Pedroso  1 ,  Veridiana Munford  2 ,  André Uchimura Bastos  2 ,  Ligia Pereira de Castro  2 ,  Victor Hugo Rocha Marussi  3 ,  Gisele Sampaio Silva  4 ,  Juliana Harumi Arita  5 ,  Carlos F M Menck  2 ,  Orlando G Barsottini  6
Affiliations
  • 1. Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, São Paulo, SP, Brazil; Hospital Israelita Albert Einstein (HIAE), São Paulo, Brazil. Electronic address: [email protected].
  • 2. Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, SP, Brazil.
  • 3. Medimagem, Beneficência Portuguesa Hospital, São Paulo, Brazil.
  • 4. Hospital Israelita Albert Einstein (HIAE), São Paulo, Brazil.
  • 5. Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
  • 6. Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, São Paulo, SP, Brazil; Hospital Israelita Albert Einstein (HIAE), São Paulo, Brazil.
PMID: 28716252 DOI: 10.1016/j.jns.2017.06.027