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High intra-familiar clinical variability in MORC2 mutated CMT2 patients.
Semplicini, Claudio; Ollagnon-Roman, Elisabeth; Leonard-Louis, Sarah; Piguet-Lacroix, Guenaelle; Silvestre, Manon; Latour, Philippe; Stojkovic, Tanya.
Affiliation
  • Semplicini C; G-H Pitié-Salpêtrière, Institut de Myologie, centre de référence des maladies neuromusculaires Paris Est, France.
  • Ollagnon-Roman E; Department of Neuroscience, University of Padova, Padova, Italy.
  • Leonard-Louis S; Service de Neurogénétique, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, Lyon, France.
  • Piguet-Lacroix G; G-H Pitié-Salpêtrière, Institut de Myologie, centre de référence des maladies neuromusculaires Paris Est, France.
  • Silvestre M; Service de Neurobiologie, Centre de Biologie Est, Hospices Civils de Lyon, Lyon, France.
  • Latour P; Service de Neurobiologie, Centre de Biologie Est, Hospices Civils de Lyon, Lyon, France.
  • Stojkovic T; Service de Neurobiologie, Centre de Biologie Est, Hospices Civils de Lyon, Lyon, France.
Brain ; 140(4): e21, 2017 04 01.
Article in En | MEDLINE | ID: mdl-28334961
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Mutation Limits: Humans Language: En Journal: Brain Year: 2017 Document type: Article Affiliation country: France
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Mutation Limits: Humans Language: En Journal: Brain Year: 2017 Document type: Article Affiliation country: France