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Semi-dominant mutations in MFN2-related neuropathy and implications for genetic counselling.
Tomaselli, Pedro J; Rossor, Alexander M; Polke, James M; Poh, Roy; Blake, Julian; Reilly, Mary M.
Affiliation
  • Tomaselli PJ; MRC Centre for Neuromuscular Diseases and National Hospital for Neurology and Neurosurgery, UCL Institute of Neurology, London, UK.
  • Rossor AM; MRC Centre for Neuromuscular Diseases and National Hospital for Neurology and Neurosurgery, UCL Institute of Neurology, London, UK.
  • Polke JM; Department of Neurogenetics, The National Hospital for Neurology and Neurosurgery, UCL Institute of Neurology, London, UK.
  • Poh R; Department of Neurogenetics, The National Hospital for Neurology and Neurosurgery, UCL Institute of Neurology, London, UK.
  • Blake J; MRC Centre for Neuromuscular Diseases and National Hospital for Neurology and Neurosurgery, UCL Institute of Neurology, London, UK.
  • Reilly MM; Department of Clinical Neurophysiology, Norfolk and Norwich University Hospital, Norwich, UK.
J Peripher Nerv Syst ; 21(1): 52-4, 2016 Mar.
Article in En | MEDLINE | ID: mdl-26930221
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Genetic Counseling Limits: Humans Language: En Journal: J Peripher Nerv Syst Journal subject: NEUROLOGIA Year: 2016 Type: Article Affiliation country: United kingdom
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Genetic Counseling Limits: Humans Language: En Journal: J Peripher Nerv Syst Journal subject: NEUROLOGIA Year: 2016 Type: Article Affiliation country: United kingdom