Produção Nacional
Revisado por pares
A new phenotype associated with homozygous GRN mutations: complicated spastic paraplegia
2016; Wiley; Volume: 24; Issue: 1 Linguagem: Inglês
10.1111/ene.13194
ISSN1468-1331
AutoresIngrid Faber, Joana Rosa Marques Prota, Alberto Martínez, Íscia Lopes‐Cendes, Marcondes C. França,
Tópico(s)Parkinson's Disease Mechanisms and Treatments
ResumoEuropean Journal of NeurologyVolume 24, Issue 1 p. e3-e4 Letter to the Editor A new phenotype associated with homozygous GRN mutations: complicated spastic paraplegia I. Faber, I. Faber Department of Neurology, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorJ. R. M. Prota, J. R. M. Prota Department of Medical Genetics, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorA. R. M. Martinez, A. R. M. Martinez Department of Neurology, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorI. Lopes-Cendes, I. Lopes-Cendes Department of Medical Genetics, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorM. C. França Júnior, Corresponding Author M. C. França Júnior mcfrancajr@uol.com.br Department of Neurology, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilCorrespondence: Marcondes C. França Júnior, MD, PhD, Department of Neurology, University of Campinas – UNICAMP, Rua Tessália Vieira de Camargo 126, Cidade Universitária ‘Zeferino Vaz’ Campinas, SP, CEP13083-887, Brazil (tel.: +55 19 3521 9217; fax: +55 19 3521 7933; e-mail: mcfrancajr@uol.com.br).Search for more papers by this author I. Faber, I. Faber Department of Neurology, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorJ. R. M. Prota, J. R. M. Prota Department of Medical Genetics, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorA. R. M. Martinez, A. R. M. Martinez Department of Neurology, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorI. Lopes-Cendes, I. Lopes-Cendes Department of Medical Genetics, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorM. C. França Júnior, Corresponding Author M. C. França Júnior mcfrancajr@uol.com.br Department of Neurology, School of Medical Sciences, University of Campinas – UNICAMP, Campinas, SP, BrazilCorrespondence: Marcondes C. França Júnior, MD, PhD, Department of Neurology, University of Campinas – UNICAMP, Rua Tessália Vieira de Camargo 126, Cidade Universitária ‘Zeferino Vaz’ Campinas, SP, CEP13083-887, Brazil (tel.: +55 19 3521 9217; fax: +55 19 3521 7933; e-mail: mcfrancajr@uol.com.br).Search for more papers by this author First published: 21 December 2016 https://doi.org/10.1111/ene.13194Citations: 16Read 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, Issue1January 2017Pages e3-e4 RelatedInformation
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