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Reply: A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy.
Ylikallio, Emil; Woldegebriel, Rosa; Tyynismaa, Henna.
Affiliation
  • Ylikallio E; Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland.
  • Woldegebriel R; Clinical Neurosciences, Neurology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Tyynismaa H; Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland.
Brain ; 141(9): e67, 2018 09 01.
Article in En | MEDLINE | ID: mdl-29982292
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Full text: 1 Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Intellectual Disability Limits: Humans Language: En Journal: Brain Year: 2018 Type: Article Affiliation country: Finland
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Full text: 1 Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Intellectual Disability Limits: Humans Language: En Journal: Brain Year: 2018 Type: Article Affiliation country: Finland