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- W2588328252 abstract "European Journal of NeurologyVolume 24, Issue 3 p. e15-e16 Letter to the Editor Targeted exomes reveal simultaneous MFN2 and GDAP1 mutations in a severe Charcot-Marie-Tooth disease type 2 phenotype C. Anghelescu, C. Anghelescu Pediatric Clinical Trials Department, I-Motion, ParisThese authors contributed equally to this work.Search for more papers by this authorB. Francou, B. Francou Laboratoire de Génétique Moléculaire, Pharmacogénétique et Hormonologie Hôpital Bicêtre, Paris-Sud, Le Kremlin-Bicêtre Plateforme d'Expertise Maladies Rares Paris Sud, Le Kremlin BicêtreThese authors contributed equally to this work.Search for more papers by this authorR. Cardas, R. Cardas Pediatric Clinical Trials Department, I-Motion, ParisSearch for more papers by this authorA. Guiochon-Mantel, A. Guiochon-Mantel Laboratoire de Génétique Moléculaire, Pharmacogénétique et Hormonologie Hôpital Bicêtre, Paris-Sud, Le Kremlin-Bicêtre Plateforme d'Expertise Maladies Rares Paris Sud, Le Kremlin BicêtreSearch for more papers by this authorP. Aubourg, P. Aubourg Service de Neuropédiatrie et Inserm 1169, Le Kremlin Bicêtre, FranceSearch for more papers by this authorL. Servais, L. Servais Pediatric Clinical Trials Department, I-Motion, ParisSearch for more papers by this authorT. Gidaro, Corresponding Author T. Gidaro t.gidaro@institut-myologie.org Pediatric Clinical Trials Department, I-Motion, ParisCorrespondence: Dr T. Gidaro, I-Motion – Pediatric Clinical Trials Department, Hôpital Armand Trousseau, Bâtiment Lemariey – Porte 20, 2ème étage, 26 Avenue du Dr Arnold Netter, 75012 Paris, France (tel.: + 33 (0)1 71 73 80 42; fax: + 33 (0)1 44 73 65 83; e-mail: t.gidaro@institut-myologie.org).Search for more papers by this author C. Anghelescu, C. Anghelescu Pediatric Clinical Trials Department, I-Motion, ParisThese authors contributed equally to this work.Search for more papers by this authorB. Francou, B. Francou Laboratoire de Génétique Moléculaire, Pharmacogénétique et Hormonologie Hôpital Bicêtre, Paris-Sud, Le Kremlin-Bicêtre Plateforme d'Expertise Maladies Rares Paris Sud, Le Kremlin BicêtreThese authors contributed equally to this work.Search for more papers by this authorR. Cardas, R. Cardas Pediatric Clinical Trials Department, I-Motion, ParisSearch for more papers by this authorA. Guiochon-Mantel, A. Guiochon-Mantel Laboratoire de Génétique Moléculaire, Pharmacogénétique et Hormonologie Hôpital Bicêtre, Paris-Sud, Le Kremlin-Bicêtre Plateforme d'Expertise Maladies Rares Paris Sud, Le Kremlin BicêtreSearch for more papers by this authorP. Aubourg, P. Aubourg Service de Neuropédiatrie et Inserm 1169, Le Kremlin Bicêtre, FranceSearch for more papers by this authorL. Servais, L. Servais Pediatric Clinical Trials Department, I-Motion, ParisSearch for more papers by this authorT. Gidaro, Corresponding Author T. Gidaro t.gidaro@institut-myologie.org Pediatric Clinical Trials Department, I-Motion, ParisCorrespondence: Dr T. Gidaro, I-Motion – Pediatric Clinical Trials Department, Hôpital Armand Trousseau, Bâtiment Lemariey – Porte 20, 2ème étage, 26 Avenue du Dr Arnold Netter, 75012 Paris, France (tel.: + 33 (0)1 71 73 80 42; fax: + 33 (0)1 44 73 65 83; e-mail: t.gidaro@institut-myologie.org).Search for more papers by this author First published: 16 February 2017 https://doi.org/10.1111/ene.13250Citations: 5 Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume24, Issue3March 2017Pages e15-e16 RelatedInformation" @default.
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- W2588328252 title "Targeted exomes reveal simultaneous<i>MFN2</i>and<i>GDAP1</i>mutations in a severe Charcot-Marie-Tooth disease type 2 phenotype" @default.
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