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SPG4 ‐related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil

2013; Wiley; Volume: 86; Issue: 2 Linguagem: Inglês

10.1111/cge.12252

1399-0004

Marcondes C. França, D.B. Dogini, Anelyssa D’Abreu, Hélio A.G. Teive, Renato P. Munhoz, Salmo Raskin, Adriana Moro, Cristina Carvalho de Melo, Amanda Pereira Gomes, Jonas Alex Morales Saute, Laura Bannach Jardim, Íscia Lopes‐Cendes,

Neurogenetic and Muscular Disorders Research

Clinical GeneticsVolume 86, Issue 2 p. 194-196 LETTER TO THE EDITOR SPG4-related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil M.C. França Jr, Corresponding Author M.C. França Jr Department of Neurology Correspondence: Marcondes C. França Jr, MD, PhD, Department of Neurology, University of Campinas—UNICAMP, Tessália Vieira de Camargo, 126, Cidade Universitaria “Zeferino Vaz”, Campinas, 13083-887, SP, Brazil Tel: +55 19 3521 9217; Fax: +55 19 3521 7933; e-mail: mcfrancajr@uol.com.brSearch for more papers by this authorD.B. Dogini, D.B. Dogini Department of Medical Genetics, School of Medical Sciences, University of Campinas—UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorA. D'Abreu, A. D'Abreu Department of NeurologySearch for more papers by this authorH.A.G. Teive, H.A.G. Teive Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorR.P. Munhoz, R.P. Munhoz Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorS. Raskin, S. Raskin Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorA. Moro, A. Moro Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorC.C. Melo, C.C. Melo Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorA.P. Gomes, A.P. Gomes Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorJ.A.M. Saute, J.A.M. Saute Medical Genetics Service, Hospital de Clinicas de Porto AlegreSearch for more papers by this authorL.B. Jardim, L.B. Jardim Medical Genetics Service, Hospital de Clinicas de Porto Alegre Department of Internal Medicine, Universidade Federal do Rio Grande do Sul, Porto Alegre, 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 author M.C. França Jr, Corresponding Author M.C. França Jr Department of Neurology Correspondence: Marcondes C. França Jr, MD, PhD, Department of Neurology, University of Campinas—UNICAMP, Tessália Vieira de Camargo, 126, Cidade Universitaria “Zeferino Vaz”, Campinas, 13083-887, SP, Brazil Tel: +55 19 3521 9217; Fax: +55 19 3521 7933; e-mail: mcfrancajr@uol.com.brSearch for more papers by this authorD.B. Dogini, D.B. Dogini Department of Medical Genetics, School of Medical Sciences, University of Campinas—UNICAMP, Campinas, SP, BrazilSearch for more papers by this authorA. D'Abreu, A. D'Abreu Department of NeurologySearch for more papers by this authorH.A.G. Teive, H.A.G. Teive Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorR.P. Munhoz, R.P. Munhoz Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorS. Raskin, S. Raskin Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorA. Moro, A. Moro Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorC.C. Melo, C.C. Melo Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorA.P. Gomes, A.P. Gomes Movement Disorders Unit, Neurology Service, Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, BrazilSearch for more papers by this authorJ.A.M. Saute, J.A.M. Saute Medical Genetics Service, Hospital de Clinicas de Porto AlegreSearch for more papers by this authorL.B. Jardim, L.B. Jardim Medical Genetics Service, Hospital de Clinicas de Porto Alegre Department of Internal Medicine, Universidade Federal do Rio Grande do Sul, Porto Alegre, 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 author First published: 05 September 2013 https://doi.org/10.1111/cge.12252Citations: 8Read 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 onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume86, Issue2August 2014Pages 194-196 RelatedInformation